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Gamma delta T cell

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400:. Also it has been proven that VĪ³9VĪ“2 T cells in patients with Psoriasis participate in the development of the disease. The number of VĪ³9VĪ“2 T cells increase in the skin lesions of psoriasis patients but decreased in the blood. This finding indicates redistribution of VĪ³9VĪ“2 T cells from the blood to the skin compartment in psoriasis. The psoriasis severity is associated with lower level of Ī³9VĪ“2 T cells in the circulation, therefore a successful anti-psoriatic therapy leads to increase of peripheral VĪ³9VĪ“2 T cells. The major outcome is that the measurement of these cells in blood and skin lesions can be used as a marker in order to follow up the psoriasis progression. 191:, IL-17 produced by the Ī³Ī“17 T cells will stimulate stromal cells expressing the IL-17 receptor to produce IL-33 in vivo, and therefore provide a molecular link to T reg cells expressing the IL-33 receptor ST2 in the adipose tissue, so ST2+ Treg cells will accumulate and this will lead to the maintenance of tissue homeostasis. This recent finding explains the mechanism by which the number of T reg cells continuously increases during aging. On the other hand, it has been shown that, after exposing mice to cold, the production of TNF and IL-17 will act on the adipocytes uncoupling the protein 1068:). In most instances, the stimuli that trigger Vd1 expansion are not derived from pathogens but instead correspond to endogenous gene products presumably upregulated on infection. The antigens recognized by non-VĪ“2 T cells expanded in the above infectious contexts have not been characterized, but the fact that VĪ“1 T-cell responses are not blocked by monoclonal antibody directed against known classical or non-classical MHC molecules suggests recognition of a new class of conserved stress-induced antigens. A recent study of primary 727: 881:, and incidentally act as VĪ³9/VĪ“2 T cell receptor agonists. However, increasing evidence suggests that these aminobisphosphonate 'antigens' are not recognised directly by VĪ³9/VĪ“2 T cells and in fact act indirectly, via their effects on the mevalonate biosynthetic pathway, leading to an accumulation of IPP. Finally, certain alkylated 574:
writers do not indicate which system they use. For example, the IMGT (International Immunogenetics Information System) uses the Heilig notation, but does not indicate this fact on its website. This table refers to variable chain VĪ³ gene segments and to monoclonal antibodies that detect the corresponding VĪ³ protein chains. Note that
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class I and II or CD1 are required for Ī³Ī“ T cell activation suggesting the existence of a novel presenting element. Strong support for a direct recognition of non-peptide antigens by the VĪ³9/VĪ“2 TCR comes from studies which demonstrated that a transfected VĪ³9/VĪ“2 TCR can confer responsiveness onto a
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are unique to humans and primates and represent a minor and unconventional constituent of the leukocyte population in peripheral blood (0.5-5%), yet they are assumed to play an early and essential role in sensing 'danger' by invading pathogens as they expand dramatically in many acute infections and
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This table summarizes the nomenclature of mouse VĪ³ chains and indicates monoclonal antibodies often used to identify these chains. This system has been best described in strain C57BL/6 and might not apply well to other strains. There are two systems of nomenclature in use (Heilig; Garman), and many
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in acute infections. It was recently discovered that Ī³Ī“17 T cells can produce IL-17 even when the immune response is not induced. These cells are likely to be generated from fetal Ī³Ī“ thymocytes and as they egress from the thymus, they will progress to non-lymphoid tissues such as lungs, peritoneal
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Recent work has shown that human VĪ³9/VĪ“2 T cells are also capable of phagocytosis, a function previously exclusive to innate myeloid lineage cells such as neutrophils, monocytes and dendritic cells This provides further evidence that the biology of Ī³Ī“ T cells spans both innate and adaptive immune
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The conditions that lead to responses of Ī³Ī“ T cells are not fully understood, and current concepts of them as 'first line of defense', 'regulatory cells', or 'bridge between innate and adaptive responses' only address facets of their complex behavior. In fact, Ī³Ī“ T cells form an entire lymphocyte
227:. They also interact with other innate and adaptive immune cells and modulate their functions. Ī³Ī“ T cell enhance or suppress inflammation, depending on the site and stage of disease. They rise from periphery and can be accumulated in inflamed tissue. These T cells can become active without 109:
and in the periphery. When mature, they develop into functionally distinct subsets that obey their own (mostly unknown) rules and have countless direct and indirect effects on healthy tissues and immune cells, pathogens and tissues enduring infections, and the host responses to them.
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class-I-chain-related gene A (MICA) has also been proposed as an important tumor antigen recognized by VĪ“1 T cells. However, the very low affinity of MICAā€“VĪ“1 TCR interactions estimated by surface plasmon resonance analyses raises doubts about the functional relevance of MICA or MHC
148:. For example, according to this paradigm, large numbers of (human) VĪ³9/VĪ“2 T cells respond within hours to common molecules produced by microbes, and highly restricted intraepithelial VĪ“1 T cells will respond to stressed epithelial cells bearing sentinels of danger. 296:, are damaged by autoreactive T cells. There is infiltration of both innate and adaptive immune cells in pancreas. Studies on mice showed that Ī³Ī“ T cells play a role in T1D pathogenesis. They infiltrate islets and may even co-operate with Ī±Ī² T cells to induce T1D. 269:. This cytokine induces Th17 cells differentiation, and dendritic cell- mediated production of IL-12 and IL-23 promotes differentiation of Th17 cells to Th1 cells, which produce IFNā€Ī³. Matrix metalloproteinases and NO present in inflamed tissue damage and degrade 578:'s proposed nomenclature is not widely used, leaving considerable confusion in the literature. One advantage and weakness of the Hayday nomenclature is that it is based on the gene order in the B6 genome, but this might not apply to other strains. 38:
chains called Ī± (alpha) and Ī² (beta) TCR chains. In contrast, Ī³Ī“ T cells have a TCR that is made up of one Ī³ (gamma) chain and one Ī“ (delta) chain. This group of T cells is usually less common than Ī±Ī² T cells. Their highest abundance is in the gut
1098:. These receptors are expressed almost exclusively by natural killer (NK) cells and play a central role in triggering their activation, but it has been described that Ī³Ī“ T cells can express these receptors. These cells are named NKp46+/VĪ“1 IELs. 222:
is important for development and progression of autoimmune diseases. Main sources are Th17 CD4+ Ī±Ī² T cells, but Ī³Ī“ T cell subset plays role in autoimmune pathogenesis and regulation, too, because they contribute to production of IL-17A and other
246:. They regulate immunosuppressive functions of IELs and play role in development of tolerance. These so-called protective Ī³Ī“ T cells promote tissue repair and cell healing. Pathogens and other inflammation stimuli cause production of 1040:, MHC-like, or non-MHC molecules suggest recognition of a highly diverse and heterogeneous set of antigens by non-VĪ“2 cells, although cognate interactions between non-VĪ“2 TCRs and any of these antigens have not been shown yet. 860:
is reduced 10,000-fold; whether IPP represents a physiological 'danger' signal of stressed or transformed cells is still unclear. Of pharmacological interest and with bioactivities comparable to that of IPP are synthetic
440:. Therefore, the effectiveness of immunotherapy based on Ī³Ī“ T cells is limited. Their invariant nature implies that immunotherapies that rely on them would not require customization for individual patients. 2672:
Thedrez A, Sabourin C, Gertner J, Devilder MC, Allain-Maillet S, FourniĆ© JJ, et al. (February 2007). "Self/non-self discrimination by human gammadelta T cells: simple solutions for a complex issue?".
180:, therefore they are able to control the maintenance of core body temperature. Using aging mice as a model, the molecular and cellular mechanisms that act under thermoneutrality circumstances ( 2347:"The bisphosphonate acute phase response: rapid and copious production of proinflammatory cytokines by peripheral blood gd T cells in response to aminobisphosphonates is inhibited by statins" 88:
compartment of mice skin. Originally referred to as Thy-1+ dendritic epidermal cells (Thy1+DEC), these cells are more commonly known as dendritic epidermal T cells (DETC). DETCs arise during
1109:. It is acknowledged that this subset can control the metastasis, so the higher levels of this population, the less probabilities for the tumor to progress and proliferate to other tissues. 960:. So the stimulation of VĪ³9VĪ“2 T cells with phosphoantigens results in expression of multiple markers which are associated with APC, like MHC I and II molecules, co-stimulatory molecules ( 1105:, in order to follow-up its progression. Lower frequencies of NKp46+/VĪ“1 IELs in healthy intestinal tissues surrounding the tumor mass, associate with a higher tumor progression and 396:
play an essential role in the disease development. In response to IL-23, the adipose gamma T cells will produce IL-17, and this interleukin promotes development and progression of
980:). Thus activated VĪ³9VĪ“2 T cells behave like APCs (Ī³Ī“ T-APC) and present antigens to Ī±Ī² T cells. This leads to turn of naĆÆve CD4+ and CD8+ Ī±Ī² T cells into effector cells. The 3153: 900:
bind directly to the VĪ³9/VĪ“2 TCR or if a presenting element exists. There is evidence for a requirement for a species-specific cell-cell contact. However, none of the known
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or autoreactive T cells is present during such disease. The role of Ī³Ī“ T cell in autoimmune disease is to help B cells to produce autoantibodies, through proinflammatory
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hitherto unresponsive cell; furthermore, antibodies to the Ī³Ī“ TCR block recognition. Thus, the presence of a functional VĪ³9/VĪ“2 TCR appears mandatory for a response to
129:, where B and T cells coordinate a slower but highly antigen-specific immune response leading to long-lasting memory against subsequent challenges by the same antigen. 380:. In the mice models, different subsets of Ī³Ī“ T cells were identified. The most abundant were the ones producing IL-17. IL-17 induces Th17 cells and Th17 response. 428:) showed that they are tolerated and safe, but some studies report that Ī³Ī“ T cells cause cancer development for example through production of IL-17 in the 476: 3146: 1342:
Morita CT, Mariuzza RA, Brenner MB (2000). "Antigen recognition by human gamma delta T cells: pattern recognition by the adaptive immune system".
2504:"Activated gammadelta T cells express the natural cytotoxicity receptor natural killer p 44 and show cytotoxic activity against myeloma cells" 2783: 2553:"NKp46-expressing human gut-resident intraepithelial VĪ“1 T cell subpopulation exhibits high antitumor activity against colorectal cancer" 3002: 2117:"Regulatory and effector functions of gamma-delta (Ī³Ī“) T cells and their therapeutic potential in adoptive cellular therapy for cancer" 523:) and CD86-CTLA-4 interaction between APCs and Ī³Ī“ T cells. They also impair effector immune cells (DC, NK, iNKT, CD8+ T cells) through 3139: 1193: 140:
to produce junctional diversity and can develop a memory phenotype. However, the various subsets may also be considered part of the
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Barros MS, de AraĆŗjo ND, MagalhĆ£es-Gama F, Pereira Ribeiro TL, Alves Hanna FS, TarragĆ“ AM, et al. (22 September 2021).
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RA is a chronic autoimmune disease caused by accumulation of self-reactive T cells, which are induced by inflammation in
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Garman RD, Doherty PJ, Raulet DH (June 1986). "Diversity, rearrangement, and expression of murine T cell gamma genes".
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activity, a process describing the uptake of exogenous antigen and its routing to the MHC I pathway for induction CD8+
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The major outcome of this study is the clinical relevance of this cells, which can be used a prognostic marker in the
1789:"Identification of a novel proinflammatory human skin-homing VĪ³9VĪ“2 T cell subset with a potential role in psoriasis" 121:, Ī³Ī“ T cells exhibit several characteristics that place them at the border between the more evolutionarily primitive 54:
molecules that activate Ī³Ī“ T cells are largely unknown. Ī³Ī“ T cells are peculiar in that they do not seem to require
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Heilig JS, Tonegawa S (1986). "Diversity of murine gamma genes and expression in fetal and adult T lymphocytes".
918: 849: 803: 996:. But in the case of a low Ī³Ī“ T-APC: CD4+ ratio it leads to differentiation of some naĆÆve Ī±Ī² T cells into Th2 ( 981: 2869: 242:Ī³Ī“ T cells are a major T cell subset of intraepithelial lymphocytes (IEL) present in the epithelial layer of 3489: 3247: 3110: 2502:
von Lilienfeld-Toal M, Nattermann J, Feldmann G, Sievers E, Frank S, Strehl J, Schmidt-Wolf IG (June 2006).
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de AraĆŗjo ND, Gama FM, de Souza Barros M, Ribeiro TL, Alves FS, Xabregas LA, et al. (7 January 2021).
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Mouse Vgamma locus for C57BL/6 genome; drawn to scale. Chromosome 13: 1.927 to 1.440 Megabp Heilig notation
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Born WK, Reardon CL, O'Brien RL (February 2006). "The function of gammadelta T cells in innate immunity".
1148: 1087: 821: 799: 472: 429: 133: 126: 3458: 3314: 3292: 2992: 2969: 2945: 1138: 512: 118: 1477:"Ī³Ī“ T cells producing interleukin-17A regulate adipose regulatory T cell homeostasis and thermogenesis" 1094:(intraepithelial lymphocytes) which express high levels of a natural cytotoxic receptor (NCR) which is 3475: 3408: 3319: 3243: 3016: 2833: 2769: 2453:"Characterization of Adaptive Ī³Ī“ T Cells in Ugandan Infants During Primary Cytomegalovirus Infection" 2173: 1143: 910: 901: 897: 413: 141: 122: 89: 77:
antigen recognition. They are of an invariant nature. They may be triggered by alarm signals such as
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although the basis for the huge differences in bioactivity between closely related molecules like
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Kohlgruber AC, Gal-Oz ST, LaMarche NM, Shimazaki M, Duquette D, Koay HF, et al. (May 2018).
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Non-VĪ“2 Ī³Ī“ T cells are expanded in various infectious contexts involving intracellular bacteria (
1001: 825: 377: 203: 78: 55: 2608:(April 2000). " cells: a right time and a right place for a conserved third way of protection". 889:, however only at millimolar concentrations, i.e. with potencies 10-10-fold lower than those of 2451:
Tuengel J, Ranchal S, Maslova A, Aulakh G, Papadopoulou M, Drissler S, et al. (Oct 2021).
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Laggner U, Di Meglio P, Perera GK, Hundhausen C, Lacy KE, Ali N, et al. (September 2011).
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response, in the most of cases to pro-inflammatory Th1 response with subsequent production of
953: 173: 1000:) or Th0 (IL-4 plus IFN-Ī³) cells. Human VĪ³9VĪ“2 T cells are also cells with excellent antigen 3582: 3523: 3463: 3435: 3430: 3398: 3385: 3375: 2921: 2897: 2725: 2682: 2650: 2617: 2572: 2564: 2523: 2515: 2474: 2464: 2415: 2407: 2366: 2358: 2309: 2270: 2224: 2181: 2128: 2087: 2077: 2011: 2003: 1954: 1913: 1903: 1862: 1852: 1808: 1800: 1759: 1749: 1708: 1700: 1689:"Ī³Ī“ T cells are essential effectors of type 1 diabetes in the nonobese diabetic mouse model" 1655: 1611: 1601: 1549: 1541: 1496: 1488: 1447: 1439: 1398: 1351: 1316: 1271: 1230: 1181: 1133: 496: 480: 361: 92:
and express an invariant and canonical VĪ³3 VĪ“1 T-cell receptor (using Garman nomenclature).
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Mikulak J, Oriolo F, Bruni E, Roberto A, Colombo FS, Villa A, et al. (December 2019).
1992:"Expansion and functions of myeloid-derived suppressor cells in the tumor microenvironment" 726: 3418: 2913: 2261:(2000). " cells: a right time and a right place for a conserved third way of protection". 1684: 1069: 1065: 862: 417: 251: 228: 168:
The Ī³Ī“17 T that will accumulate in the adipose tissue (dermis) will not only controls the
34:(TCR) on their surface. Most T cells are Ī±Ī² (alpha beta) T cells with TCR composed of two 31: 1387:"Human gamma delta T cells: a lymphoid lineage cell capable of professional phagocytosis" 262:
is responsible for cell-mediated production of antimicrobial peptides and tissue repair.
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and high cytokine secretion of Ī³Ī“ T cells suggest that these cells can be effective in
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Holtmeier W, Kabelitz (2005). "Ī“Ī“ T Cells Link Innate and Adaptive Immune Responses".
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and ubiquitously present in all living cells (including human cells), yet its potency
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Wu Y, Wu W, Wong WM, Ward E, Thrasher AJ, Goldblatt D, et al. (November 2009).
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and induction of anti-tumor response. Ī³Ī“ T cells also interact with DCs and develop
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infection in infants found increased VĪ“1 T cells that also expressed the typically
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Psoriasis is one of the autoimmune diseases in which the Ī³Ī“ T cells together with
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These VĪ³9VĪ“2 T cells can also behave like professional antigen-presenting cells (
846:, are unable to produce HMB-PP and do not specifically activate VĪ³9/VĪ“2 T cells. 3115: 2818: 2813: 957: 870: 866: 776: 768: 544: 540: 464: 460: 425: 333: 329: 321: 317: 313: 169: 125:
that permits a rapid beneficial response to a variety of foreign agents and the
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Papotto PH, Silva-Santos B (May 2018). "Got my Ī³Ī“17 T cells to keep me warm".
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parasites, but is absent from the human host. Bacterial species that lack the
511:Ī³Ī“ T cells perform a regulatory and suppressive role in the TME expression of 452: 337: 285: 224: 102: 2737: 2345:
Hewitt RE, Lissina A, Green AE, Slay ES, Price DA, Sewell AK (January 2005).
1804: 1754: 1704: 1660: 1643: 1606: 1443: 1403: 1386: 952:). It means that the stimulation with IPP or HMB-PP induces migration to the 921:
cannot be explained by conventional epitope presentation/recognition models.
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Eberl M, Hintz M, Reichenberg A, Kollas AK, Wiesner J, Jomaa H (June 2003).
772: 468: 456: 397: 357: 356:Ī³Ī“ T cells are involved in development of this autoimmune disease. They are 345: 215: 2745: 2694: 2664: 2655: 2638: 2629: 2586: 2537: 2488: 2429: 2380: 2323: 2282: 2142: 2101: 2082: 2025: 1968: 1927: 1876: 1822: 1773: 1722: 1669: 1625: 1563: 1510: 1461: 1412: 1363: 1328: 1285: 1203: 113:
Like other 'unconventional' T cell subsets bearing invariant TCRs, such as
2298:"Microbial isoprenoid biosynthesis and human gammadelta T cell activation" 2236: 2193: 1959: 1942: 1355: 1244: 790:
Of note, all VĪ³9/VĪ“2 T cells recognize the same small microbial compound (
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ligand ā€“ they can induce inflammation in autoimmune diseases very fast.
3556: 3370: 3219: 3190: 3076: 1554: 817: 784: 535:. Also IL-17 secreted by Ī³Ī“ T cells has pro-tumorogenic role (enhanced 293: 195:, which is required for inducing a UCP1-dependent thermogenic program. 66: 63: 51: 2469: 2133: 2116: 1185: 928:). It seems that human VĪ³9VĪ“2 T cells are characterized by a specific 160:
Recently, it was believed that Ī³Ī“17 T cells were only able to produce
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Bergstresser PR, Sullivan S, Streilein JW, Tigelaar RE (July 1985).
1008:. Thus activated cytotoxic T cells can effectively kill infected or 308:
and joints. RA patients have higher numbers of Ī³Ī“ T cells producing
234:Ī³Ī“ T cells have clinical association with many autoimmune diseases. 1260:"Skin gammadelta T-cell functions in homeostasis and wound healing" 1180:. Chemical Immunology and Allergy. Vol. 86. pp. 151ā€“183. 376:, and these cells accumulate in demyelinated areas of CNS and make 1590:"Ī³Ī“ T Lymphocytes: An Effector Cell in Autoimmunity and Infection" 1095: 1077: 1009: 969: 937: 882: 745: 725: 516: 492: 369: 365: 325: 74: 1841:"Ī³Ī“ T Cells for Leukemia Immunotherapy: New and Expanding Trends" 1219:"Origin and function of Thy-1+ dendritic epidermal cells in mice" 932:
migration program, including multiple receptors for inflammatory
893:, thereby raising questions about their physiological relevance. 810:
is an essential metabolite in most pathogenic bacteria including
1892:"Gamma-delta (Ī³Ī“) T cells: friend or foe in cancer development?" 1081: 977: 973: 965: 961: 949: 945: 941: 436:
and cell growth or because their ability to increase numbers of
393: 341: 192: 3135: 2765: 2639:"Immunosurveillance and immunoregulation by gammadelta T cells" 2761: 1061: 443:Ī³Ī“ T cells can be divided into effector and regulatory cells: 340:
induced by inflammatory cytokines, together with RANKL, cause
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class-I-chain-related gene B (MICB) recognition by VĪ“1 TCRs.
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17D1; can detect VĪ³6VĪ“1 when pretreated with GL3 antibodies
184:) or after cold exposure have recently been acknowledged. 1736:
Cruz MS, Diamond A, Russell A, Jameson JM (6 June 2018).
463:, Ī³Ī“ T cells interact with stress-induced molecules on 1738:"Human Ī±Ī² and Ī³Ī“ T Cells in Skin Immunity and Disease" 1036:
TCRs and the existence of VĪ“1 clones reactive against
312:. It leads to production of inflammatory cytokines by 73:. Ī³Ī“ T cells are believed to have a prominent role in 1683:
Markle JG, Mortin-Toth S, Wong AS, Geng L, Hayday A,
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may exceed all other lymphocytes within a few days,
3544: 3502: 3444: 3345: 3275: 3183: 3176: 3101: 3024: 3015: 2983: 2878: 2799: 1086:A recent study has identified a specific subset of 580: 368:. Patients have increased numbers of Ī³Ī“ T cells in 2711: 1644:"Role of gamma-delta (Ī³Ī“) T cells in autoimmunity" 101:system that develops under the influence of other 613:536; 17D1 specific for VĪ³5(Heilig)+VĪ“1 clonotype 364:, cells that participate in the myelinization of 265:On the other hand, pathogenic Ī³Ī“ T cells produce 885:have been described to activate VĪ³9/VĪ“2 T cells 1637: 1635: 1583: 1581: 794:)-4-hydroxy-3-methyl-but-2-enyl pyrophosphate ( 483:deposited on tumor cells). Ī³Ī“ T cells secrete 467:and secrete cytotoxic molecules, inflammatory 43:, within a population of lymphocytes known as 3147: 2777: 1056:) as well as extracellular bacteria, such as 84:A Ī³Ī“-T-cell sub-population exists within the 8: 2396:"Ī³Ī“ T-APCs: a novel tool for immunotherapy?" 451:After infiltrating a tumor as a response to 332:(RANKL causes conversion of precursors into 132:Ī³Ī“ T cells may be considered a component of 1588:Shiromizu CM, Jancic CC (16 October 2018). 1171: 1169: 3180: 3154: 3140: 3132: 3021: 2884: 2784: 2770: 2762: 852:itself is structurally closely related to 144:in which a specific TCR can function as a 2654: 2576: 2527: 2478: 2468: 2419: 2370: 2313: 2132: 2091: 2081: 2015: 1958: 1917: 1907: 1866: 1856: 1812: 1763: 1753: 1712: 1659: 1615: 1605: 1553: 1500: 1451: 1402: 1275: 1234: 984:, induced by Ī³Ī“ T-APC, most often led to 475:cells. They can also lyse tumor cells by 2643:The Journal of Investigative Dermatology 1990:Qu P, Wang LZ, Lin PC (September 2016). 1426:Chien YH, Zeng X, Prinz I (April 2013). 1223:The Journal of Investigative Dermatology 873:(Aredia), that are widely used to treat 477:antibodyā€dependent cellular cytotoxicity 348:erosion, which leads to RA development. 1834: 1832: 1165: 1258:Jameson J, Havran WL (February 2007). 1028:The extensive structural diversity of 491:, which leads to higher expression of 1890:Zhao Y, Niu C, Cui J (January 2018). 956:, specifically to the T cell area of 824:and synthesize IPP via the classical 479:(ADCC) (through binding Fc region of 7: 2508:Clinical and Experimental Immunology 2400:Cellular and Molecular Life Sciences 2351:Clinical and Experimental Immunology 1344:Springer Seminars in Immunopathology 1012:cells. This fact can be used in the 896:It is still not clear whether these 3003:Mucosal associated invariant T cell 688:peripheral lymphoid tissues;JĪ³4CĪ³4 254:, it induces Ī³Ī“ T cells to produce 165:cavity, dermis, tongue and uterus. 667:most common form in intestinal IEL 555:Gene families in different species 408:Non-MHC restricted recognition of 206:results from abnormal response of 14: 1896:Journal of Translational Medicine 798:), a natural intermediate of the 336:). Matrix metalloproteinases and 273:, leading to development of IBD. 3039:Lymphokine-activated killer cell 2687:10.1111/j.1600-065X.2006.00468.x 2622:10.1146/annurev.immunol.18.1.975 2520:10.1111/j.1365-2249.2006.03078.x 2363:10.1111/j.1365-2249.2005.02665.x 2275:10.1146/annurev.immunol.18.1.975 2115:Paul S, Lal G (September 2016). 1277:10.1111/j.1600-065X.2006.00483.x 1178:Mechanisms of Epithelial Defense 543:, expansion and polarization of 438:myeloid derived suppressor cells 60:major-histocompatibility-complex 2121:International Journal of Cancer 1642:Paul S, Lal G (February 2015). 284:is an autoimmune disease where 238:Inflammatory bowel diseases IBD 3481:Immunoglobulin class switching 2394:Moser B, Eberl M (July 2011). 2070:Journal of Immunology Research 2039:Irving, Michael (2023-11-13). 1947:European Journal of Immunology 416:. Trials in numerous cancers ( 1: 2315:10.1016/S0014-5793(03)00483-6 1309:Current Opinion in Immunology 3084:Type 3 innate lymphoid cells 3072:Type 2 innate lymphoid cells 3067:Type 1 innate lymphoid cells 3054:Uterine natural killer cells 3034:Cytokine-induced killer cell 2229:10.1016/0092-8674(86)90787-7 2008:10.1016/j.canlet.2015.10.022 1941:Silva-Santos B (July 2010). 1648:Journal of Leukocyte Biology 1236:10.1111/1523-1747.ep12275516 146:pattern recognition receptor 96:Innate and adaptive immunity 2710:Dolgin, Elie (2022-06-01). 2610:Annual Review of Immunology 2263:Annual Review of Immunology 633:reproductive mucosa;JĪ³1CĪ³1 45:intraepithelial lymphocytes 3599: 3310:Polyclonal B cell response 2730:10.1038/s41587-022-01363-6 2637:Girardi M (January 2006). 2569:10.1172/jci.insight.125884 968:) and adhesion receptors ( 813:Mycobacterium tuberculosis 69:, although some recognize 3062: 2887: 2412:10.1007/s00018-011-0706-6 1909:10.1186/s12967-017-1378-2 1858:10.3389/fimmu.2021.729085 1546:10.1038/s41590-018-0090-6 1493:10.1038/s41590-018-0094-2 1321:10.1016/j.coi.2005.11.007 1020:and infectious diseases. 804:isopentenyl pyrophosphate 547:and their suppression of 495:, positive regulation of 1805:10.4049/jimmunol.1100804 1755:10.3389/fimmu.2018.01304 1705:10.4049/jimmunol.1203502 1661:10.1189/jlb.3RU0914-443R 1607:10.3389/fimmu.2018.02389 1444:10.1016/j.it.2012.11.004 1404:10.4049/jimmunol.0901772 669:orthologous to human VĪ³1 3111:Hematopoietic stem cell 2870:Lymphoplasmacytoid cell 1845:Frontiers in Immunology 1742:Frontiers in Immunology 1594:Frontiers in Immunology 1103:colorectal cancer (CRC) 497:cytotoxic T lymphocytes 300:Rheumatoid arthritis RA 3424:Tolerance in pregnancy 3166:adaptive immune system 2656:10.1038/sj.jid.5700003 1149:Adaptive immune system 1139:Natural killer T cells 822:non-mevalonate pathway 800:non-mevalonate pathway 731: 430:tumor microenvironment 127:adaptive immune system 119:Natural Killer T cells 71:MHC class Ib molecules 62:(MHC) presentation of 3459:Somatic hypermutation 3293:Polyclonal antibodies 3288:Monoclonal antibodies 3017:Innate lymphoid cells 2993:Natural killer T cell 2675:Immunological Reviews 1960:10.1002/eji.201040707 1793:Journal of Immunology 1693:Journal of Immunology 1391:Journal of Immunology 1356:10.1007/s002810000042 1264:Immunological Reviews 1024:Human non-VĪ“2 T cells 911:non-peptidic antigens 898:non-peptidic antigens 729: 584:Heilig and Tonegawa's 513:transcription factors 352:Multiple sclerosis MS 176:but also an adaptive 3476:Junctional diversity 3244:Antigen presentation 2718:Nature Biotechnology 2083:10.1155/2021/6633824 1432:Trends in Immunology 1229:(1 Suppl): 85sā€“90s. 1144:Innate immune system 1058:Borrelia burgdorferi 863:aminobisphosphonates 806:(IPP) biosynthesis. 507:Regulatory functions 414:cancer immunotherapy 156:Murine thermogenesis 123:innate immune system 3471:V(D)J recombination 3454:Affinity maturation 3206:Antigenic variation 2985:Innate-like T cells 2865:Transitional B cell 2178:1986Natur.322..836H 1076:associated markers 374:cerebrospinal fluid 277:Type 1 diabetes T1D 187:When mice are in a 138:rearrange TCR genes 79:heat shock proteins 20:Gamma delta T cells 1154:Regulatory T cells 1002:cross-presentation 902:antigen-presenting 826:mevalonate pathway 732: 685:2.11 Pereira 1995 593:"Hayday's system" 447:Effector functions 204:Autoimmune disease 174:regulatory T cells 56:antigen processing 3570: 3569: 3498: 3497: 3248:professional APCs 3129: 3128: 3097: 3096: 3011: 3010: 2470:10.3390/v13101987 2406:(14): 2443ā€“2452. 2172:(6082): 836ā€“840. 2134:10.1002/ijc.30109 1699:(11): 5392ā€“5401. 1534:Nature Immunology 1481:Nature Immunology 1186:10.1159/000086659 1134:Cytotoxic T cells 1006:cytotoxic T cells 954:lymphatic tissues 828:instead, such as 740:Human VĪ“2 T cells 724: 723: 560:Laboratory mice ( 539:, recruitment of 473:adaptive immunity 432:, which promotes 134:adaptive immunity 90:fetal development 3590: 3464:Clonal selection 3436:Immune privilege 3431:Immunodeficiency 3386:Cross-reactivity 3376:Hypersensitivity 3181: 3156: 3149: 3142: 3133: 3049:Adaptive NK cell 3022: 2885: 2786: 2779: 2772: 2763: 2757: 2715: 2706: 2668: 2658: 2633: 2591: 2590: 2580: 2548: 2542: 2541: 2531: 2499: 2493: 2492: 2482: 2472: 2448: 2442: 2441: 2423: 2391: 2385: 2384: 2374: 2342: 2336: 2335: 2317: 2293: 2287: 2286: 2255: 2249: 2248: 2212: 2206: 2205: 2186:10.1038/322836a0 2161: 2155: 2154: 2136: 2112: 2106: 2105: 2095: 2085: 2061: 2055: 2054: 2052: 2051: 2036: 2030: 2029: 2019: 1987: 1981: 1980: 1962: 1953:(7): 1873ā€“1876. 1938: 1932: 1931: 1921: 1911: 1887: 1881: 1880: 1870: 1860: 1836: 1827: 1826: 1816: 1799:(5): 2783ā€“2793. 1784: 1778: 1777: 1767: 1757: 1733: 1727: 1726: 1716: 1680: 1674: 1673: 1663: 1639: 1630: 1629: 1619: 1609: 1585: 1576: 1575: 1557: 1529: 1523: 1522: 1504: 1472: 1466: 1465: 1455: 1423: 1417: 1416: 1406: 1397:(9): 5622ā€“5629. 1382: 1376: 1375: 1339: 1333: 1332: 1304: 1298: 1297: 1279: 1255: 1249: 1248: 1238: 1214: 1208: 1207: 1173: 589:Garman's system 581: 362:oligodendrocytes 292:, which produce 210:. Production of 3598: 3597: 3593: 3592: 3591: 3589: 3588: 3587: 3573: 3572: 3571: 3566: 3540: 3494: 3440: 3419:Clonal deletion 3347: 3341: 3271: 3172: 3160: 3130: 3125: 3093: 3058: 3007: 2979: 2973: 2965: 2957: 2949: 2925: 2917: 2910: 2874: 2852: 2795: 2790: 2760: 2709: 2671: 2636: 2616:(1): 975ā€“1026. 2604: 2600: 2598:Further reading 2595: 2594: 2550: 2549: 2545: 2501: 2500: 2496: 2450: 2449: 2445: 2393: 2392: 2388: 2344: 2343: 2339: 2295: 2294: 2290: 2257: 2256: 2252: 2214: 2213: 2209: 2163: 2162: 2158: 2114: 2113: 2109: 2063: 2062: 2058: 2049: 2047: 2038: 2037: 2033: 1989: 1988: 1984: 1940: 1939: 1935: 1889: 1888: 1884: 1838: 1837: 1830: 1786: 1785: 1781: 1735: 1734: 1730: 1682: 1681: 1677: 1641: 1640: 1633: 1587: 1586: 1579: 1531: 1530: 1526: 1474: 1473: 1469: 1425: 1424: 1420: 1384: 1383: 1379: 1341: 1340: 1336: 1306: 1305: 1301: 1257: 1256: 1252: 1216: 1215: 1211: 1196: 1175: 1174: 1167: 1162: 1115: 1070:cytomegalovirus 1066:cytomegalovirus 1026: 982:differentiation 904:molecules like 742: 737: 670: 668: 590: 585: 571: 569:Mouse VĪ³ chains 566: 557: 509: 449: 418:renal carcinoma 406: 386: 354: 302: 279: 252:dendritic cells 240: 201: 158: 142:innate immunity 98: 32:T-cell receptor 30:that have a Ī³Ī“ 17: 12: 11: 5: 3596: 3594: 3586: 3585: 3575: 3574: 3568: 3567: 3565: 3564: 3559: 3554: 3548: 3546: 3542: 3541: 3539: 3538: 3533: 3532: 3531: 3521: 3520: 3519: 3508: 3506: 3500: 3499: 3496: 3495: 3493: 3492: 3483: 3478: 3473: 3468: 3467: 3466: 3461: 3450: 3448: 3446:Immunogenetics 3442: 3441: 3439: 3438: 3433: 3428: 3427: 3426: 3421: 3416: 3411: 3406: 3394: 3393: 3391:Co-stimulation 3388: 3383: 3378: 3373: 3368: 3363: 3358: 3351: 3349: 3343: 3342: 3340: 3339: 3334: 3332:Immune complex 3328: 3327: 3322: 3317: 3312: 3307: 3306: 3305: 3300: 3295: 3290: 3279: 3277: 3273: 3272: 3270: 3269: 3264: 3259: 3254: 3252:Dendritic cell 3240: 3239: 3234: 3233: 3232: 3230:Conformational 3227: 3216: 3215: 3210: 3209: 3208: 3203: 3198: 3187: 3185: 3178: 3174: 3173: 3161: 3159: 3158: 3151: 3144: 3136: 3127: 3126: 3124: 3123: 3118: 3113: 3107: 3105: 3099: 3098: 3095: 3094: 3092: 3091: 3086: 3081: 3080: 3079: 3069: 3063: 3060: 3059: 3057: 3056: 3051: 3046: 3041: 3036: 3030: 3028: 3019: 3013: 3012: 3009: 3008: 3006: 3005: 3000: 2995: 2989: 2987: 2981: 2980: 2978: 2977: 2976: 2975: 2971: 2967: 2963: 2959: 2955: 2951: 2947: 2938: 2933: 2923: 2915: 2908: 2900: 2894: 2888: 2882: 2876: 2875: 2873: 2872: 2867: 2862: 2861: 2860: 2850: 2846: 2841: 2836: 2831: 2826: 2821: 2816: 2811: 2805: 2803: 2797: 2796: 2791: 2789: 2788: 2781: 2774: 2766: 2759: 2758: 2724:(6): 805ā€“808. 2707: 2681:(1): 123ā€“135. 2669: 2634: 2601: 2599: 2596: 2593: 2592: 2543: 2514:(3): 528ā€“533. 2494: 2443: 2386: 2357:(1): 101ā€“111. 2337: 2288: 2250: 2223:(5): 733ā€“742. 2207: 2156: 2127:(5): 976ā€“985. 2107: 2056: 2031: 2002:(1): 253ā€“256. 1996:Cancer Letters 1982: 1933: 1882: 1828: 1779: 1728: 1675: 1654:(2): 259ā€“271. 1631: 1577: 1540:(5): 427ā€“429. 1524: 1487:(5): 464ā€“474. 1467: 1438:(4): 151ā€“154. 1418: 1377: 1350:(3): 191ā€“217. 1334: 1299: 1250: 1209: 1194: 1164: 1163: 1161: 1158: 1157: 1156: 1151: 1146: 1141: 1136: 1131: 1129:Helper T cells 1126: 1124:Memory T cells 1121: 1114: 1111: 1090:-resident VĪ“1 1025: 1022: 837:Staphylococcus 741: 738: 736: 733: 722: 721: 720:JĪ³3-pseudoCĪ³3 718: 716: 713: 710: 706: 705: 702: 700: 697: 694: 690: 689: 686: 683: 680: 677: 673: 672: 665: 664:F2.67 Pereira 662: 659: 656: 652: 651: 648: 645: 642: 639: 635: 634: 631: 628: 625: 622: 618: 617: 614: 611: 608: 605: 601: 600: 597: 594: 591: 587: 570: 567: 565: 558: 556: 553: 508: 505: 448: 445: 405: 402: 385: 382: 353: 350: 306:synovial fluid 301: 298: 278: 275: 271:basal membrane 239: 236: 212:autoantibodies 200: 197: 157: 154: 97: 94: 15: 13: 10: 9: 6: 4: 3: 2: 3595: 3584: 3581: 3580: 3578: 3563: 3560: 3558: 3555: 3553: 3550: 3549: 3547: 3543: 3537: 3534: 3530: 3527: 3526: 3525: 3522: 3518: 3515: 3514: 3513: 3510: 3509: 3507: 3505: 3501: 3491: 3487: 3484: 3482: 3479: 3477: 3474: 3472: 3469: 3465: 3462: 3460: 3457: 3456: 3455: 3452: 3451: 3449: 3447: 3443: 3437: 3434: 3432: 3429: 3425: 3422: 3420: 3417: 3415: 3414:Clonal anergy 3412: 3410: 3407: 3405: 3402: 3401: 3400: 3396: 3395: 3392: 3389: 3387: 3384: 3382: 3379: 3377: 3374: 3372: 3369: 3367: 3364: 3362: 3359: 3357: 3353: 3352: 3350: 3344: 3338: 3335: 3333: 3330: 3329: 3326: 3323: 3321: 3318: 3316: 3313: 3311: 3308: 3304: 3303:Microantibody 3301: 3299: 3296: 3294: 3291: 3289: 3286: 3285: 3284: 3281: 3280: 3278: 3274: 3268: 3265: 3263: 3260: 3258: 3255: 3253: 3249: 3245: 3242: 3241: 3238: 3235: 3231: 3228: 3226: 3223: 3222: 3221: 3218: 3217: 3214: 3211: 3207: 3204: 3202: 3199: 3197: 3194: 3193: 3192: 3189: 3188: 3186: 3182: 3179: 3175: 3171: 3167: 3164: 3157: 3152: 3150: 3145: 3143: 3138: 3137: 3134: 3122: 3121:Prolymphocyte 3119: 3117: 3114: 3112: 3109: 3108: 3106: 3104: 3103:Lymphopoiesis 3100: 3090: 3087: 3085: 3082: 3078: 3075: 3074: 3073: 3070: 3068: 3065: 3064: 3061: 3055: 3052: 3050: 3047: 3045: 3042: 3040: 3037: 3035: 3032: 3031: 3029: 3027: 3023: 3020: 3018: 3014: 3004: 3001: 2999: 2996: 2994: 2991: 2990: 2988: 2986: 2982: 2974: 2968: 2966: 2960: 2958: 2952: 2950: 2944: 2943: 2942: 2941:Memory T cell 2939: 2937: 2934: 2931: 2927: 2919: 2911: 2904: 2901: 2899: 2898:Cytotoxic CD8 2895: 2893: 2890: 2889: 2886: 2883: 2881: 2877: 2871: 2868: 2866: 2863: 2859: 2856: 2855: 2854: 2847: 2845: 2842: 2840: 2837: 2835: 2834:Marginal zone 2832: 2830: 2827: 2825: 2822: 2820: 2817: 2815: 2812: 2810: 2807: 2806: 2804: 2802: 2798: 2794: 2787: 2782: 2780: 2775: 2773: 2768: 2767: 2764: 2755: 2751: 2747: 2743: 2739: 2735: 2731: 2727: 2723: 2719: 2714: 2708: 2704: 2700: 2696: 2692: 2688: 2684: 2680: 2676: 2670: 2666: 2662: 2657: 2652: 2648: 2644: 2640: 2635: 2631: 2627: 2623: 2619: 2615: 2611: 2607: 2603: 2602: 2597: 2588: 2584: 2579: 2574: 2570: 2566: 2562: 2558: 2554: 2547: 2544: 2539: 2535: 2530: 2525: 2521: 2517: 2513: 2509: 2505: 2498: 2495: 2490: 2486: 2481: 2476: 2471: 2466: 2462: 2458: 2454: 2447: 2444: 2439: 2435: 2431: 2427: 2422: 2417: 2413: 2409: 2405: 2401: 2397: 2390: 2387: 2382: 2378: 2373: 2368: 2364: 2360: 2356: 2352: 2348: 2341: 2338: 2333: 2329: 2325: 2321: 2316: 2311: 2308:(1ā€“3): 4ā€“10. 2307: 2303: 2299: 2292: 2289: 2284: 2280: 2276: 2272: 2268: 2264: 2260: 2254: 2251: 2246: 2242: 2238: 2234: 2230: 2226: 2222: 2218: 2211: 2208: 2203: 2199: 2195: 2191: 2187: 2183: 2179: 2175: 2171: 2167: 2160: 2157: 2152: 2148: 2144: 2140: 2135: 2130: 2126: 2122: 2118: 2111: 2108: 2103: 2099: 2094: 2089: 2084: 2079: 2075: 2071: 2067: 2060: 2057: 2046: 2042: 2035: 2032: 2027: 2023: 2018: 2013: 2009: 2005: 2001: 1997: 1993: 1986: 1983: 1978: 1974: 1970: 1966: 1961: 1956: 1952: 1948: 1944: 1937: 1934: 1929: 1925: 1920: 1915: 1910: 1905: 1901: 1897: 1893: 1886: 1883: 1878: 1874: 1869: 1864: 1859: 1854: 1850: 1846: 1842: 1835: 1833: 1829: 1824: 1820: 1815: 1810: 1806: 1802: 1798: 1794: 1790: 1783: 1780: 1775: 1771: 1766: 1761: 1756: 1751: 1747: 1743: 1739: 1732: 1729: 1724: 1720: 1715: 1710: 1706: 1702: 1698: 1694: 1690: 1687:(June 2013). 1686: 1679: 1676: 1671: 1667: 1662: 1657: 1653: 1649: 1645: 1638: 1636: 1632: 1627: 1623: 1618: 1613: 1608: 1603: 1599: 1595: 1591: 1584: 1582: 1578: 1573: 1569: 1565: 1561: 1556: 1551: 1547: 1543: 1539: 1535: 1528: 1525: 1520: 1516: 1512: 1508: 1503: 1498: 1494: 1490: 1486: 1482: 1478: 1471: 1468: 1463: 1459: 1454: 1449: 1445: 1441: 1437: 1433: 1429: 1422: 1419: 1414: 1410: 1405: 1400: 1396: 1392: 1388: 1381: 1378: 1373: 1369: 1365: 1361: 1357: 1353: 1349: 1345: 1338: 1335: 1330: 1326: 1322: 1318: 1314: 1310: 1303: 1300: 1295: 1291: 1287: 1283: 1278: 1273: 1269: 1265: 1261: 1254: 1251: 1246: 1242: 1237: 1232: 1228: 1224: 1220: 1213: 1210: 1205: 1201: 1197: 1195:3-8055-7862-8 1191: 1187: 1183: 1179: 1172: 1170: 1166: 1159: 1155: 1152: 1150: 1147: 1145: 1142: 1140: 1137: 1135: 1132: 1130: 1127: 1125: 1122: 1120: 1119:Naive T cells 1117: 1116: 1112: 1110: 1108: 1104: 1099: 1097: 1093: 1089: 1084: 1083: 1079: 1075: 1071: 1067: 1063: 1060:and viruses ( 1059: 1055: 1051: 1046: 1043: 1039: 1035: 1031: 1023: 1021: 1019: 1015: 1014:immunotherapy 1011: 1007: 1003: 999: 995: 991: 987: 986:T helper cell 983: 979: 975: 971: 967: 963: 959: 955: 951: 947: 943: 939: 935: 931: 927: 922: 920: 916: 912: 907: 903: 899: 894: 892: 888: 884: 880: 876: 872: 868: 864: 859: 855: 851: 847: 845: 844: 839: 838: 833: 832: 831:Streptococcus 827: 823: 819: 815: 814: 809: 805: 801: 797: 793: 788: 786: 782: 781:toxoplasmosis 778: 774: 770: 766: 762: 761:salmonellosis 758: 754: 749: 747: 739: 734: 728: 719: 717: 714: 711: 708: 707: 703: 701: 698: 695: 692: 691: 687: 684: 681: 678: 675: 674: 666: 663: 660: 657: 654: 653: 649: 646: 643: 640: 637: 636: 632: 629: 626: 623: 620: 619: 616:Skin, JĪ³1CĪ³1 615: 612: 609: 606: 603: 602: 598: 595: 592: 588: 583: 582: 579: 577: 576:Adrian Hayday 568: 563: 559: 554: 552: 550: 546: 542: 538: 534: 530: 526: 522: 518: 514: 506: 504: 502: 498: 494: 490: 486: 482: 478: 474: 471:and activate 470: 466: 462: 458: 454: 446: 444: 441: 439: 435: 431: 427: 423: 419: 415: 411: 403: 401: 399: 395: 391: 383: 381: 379: 375: 371: 367: 363: 359: 351: 349: 347: 343: 339: 335: 331: 327: 323: 319: 315: 311: 307: 299: 297: 295: 291: 287: 283: 276: 274: 272: 268: 263: 261: 257: 253: 249: 248:retinoic acid 245: 237: 235: 232: 230: 226: 221: 217: 213: 209: 208:immune system 205: 198: 196: 194: 190: 185: 183: 179: 178:thermogenesis 175: 171: 166: 163: 155: 153: 149: 147: 143: 139: 136:in that they 135: 130: 128: 124: 120: 116: 111: 108: 104: 95: 93: 91: 87: 82: 80: 76: 72: 68: 65: 61: 57: 53: 48: 46: 42: 37: 33: 29: 25: 21: 16:T cell subset 3381:Inflammation 3366:Alloimmunity 3361:Autoimmunity 3346:Immunity vs. 3298:Autoantibody 3196:Superantigen 2997: 2721: 2717: 2678: 2674: 2649:(1): 25ā€“31. 2646: 2642: 2613: 2609: 2560: 2556: 2546: 2511: 2507: 2497: 2463:(10): 1987. 2460: 2456: 2446: 2403: 2399: 2389: 2354: 2350: 2340: 2305: 2302:FEBS Letters 2301: 2291: 2269:: 975ā€“1026. 2266: 2262: 2253: 2220: 2216: 2210: 2169: 2165: 2159: 2124: 2120: 2110: 2073: 2069: 2059: 2048:. 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Index

T cells
T-cell receptor
glycoprotein
mucosa
intraepithelial lymphocytes
antigenic
antigen processing
major-histocompatibility-complex
peptide
epitopes
MHC class Ib molecules
lipid
heat shock proteins
epidermal
fetal development
leukocytes
thymus
CD1d
Natural Killer T cells
innate immune system
adaptive immune system
adaptive immunity
rearrange TCR genes
innate immunity
pattern recognition receptor
IL-17
homeostasis
regulatory T cells
thermogenesis
steady state

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