170:
of virosomes are the rapid detection and activation of the immune response against the viral glycoproteins, which can result in a decrease of the virosomes. However, glycoproteins can still induce a prophylactic response against the virus, which helps with establishing virosomes as vaccine delivery systems. If the virosome is administered into the bloodstream, the virosome can disintegrate. However, if the virosome can reach the target quickly enough, the drug delivery will still happen. There are some challenges with virosomes, but there are ways in which the virosome can still help activate the immune response.
44:
glycoproteins. As a drug or vaccine delivery mechanism they are biologically compatible with many host organisms and are also biodegradable. The use of reconstituted virally derived proteins in the formation of the virosome allows for the utilization of what would otherwise be the immunogenic properties of a live-attenuated virus, but is instead a safely killed virus. A safely killed virus can serve as a promising
77:. Antigens are molecules that triggers an immune response when targeted by a specific antibody that corresponds to the shape of the antigen. Haemagglutinin is a viral glycoprotein that causes red blood cell agglutination. Neuraminidase are enzymes that break glycosidic linkages. The size and surface molecules presented on of the virosome can be modified so that it can target different types of cells.
103:
65:. Glycoproteins are a type of protein that have an oligosaccharide chain bonded to amino acid chains. The different types of glycoproteins on the surface of the virosome increases the specificity of the target cells because the surface glycoproteins help with recognition as well as the attachments of the virosomes to their target cells. In the case of the influenza virosome, the glycoproteins are
20:
169:
The benefits of virosomes are that the specific structure and small size help with the precision of target cells. The phospholipid membrane protects the virosome from adverse reactions in the body and the membrane allows the virosome to be biocompatible and biodegradable in the body. The challenges
43:
are infectious agents that can replicate in their host organism, however virosomes do not replicate. The properties that virosomes share with viruses are based on their structure; virosomes are essentially safely modified viral envelopes that contain the phospholipid membrane and surface
338:
85:
Virosomes deliver antigens and therapeutic agents to their targeted cells. Virosomes can act as immunopotentiating agents and as agents of targeted drug delivery. Virosomes as immunopotentiating agents activate
412:
Bomsel M, Tudor D, Drillet AS, Alfsen A, Ganor Y, Roger MG, Mouz N, Amacker M, Chalifour A, Diomede L, Devillier G, Cong Z, Wei Q, Gao H, Qin C, Yang GB, Zurbriggen R, Lopalco L, Fleury S (25 February 2011).
60:
membrane. Inside of the virosome, there is a central cavity that holds the therapeutic molecules such as nucleic acids, proteins, and drugs. On the surface of the virosome, there can be different types of
377:
Huckriede, Anke; Bungener, Laura; Stegmann, Toon; Daemen, Toos; Medema, Jeroen; Palache, Abraham M.; Wilschut, Jan (2005). "The virosome concept for influenza vaccines".
330:
94:. Virosomes are suspended in saline buffers and are administered through respiratory, parenteral, intravenous, oral, intramuscular, and topical routes.
454:
Waelti, Ernst; Wegmann, Nina; Schwaninger, Ruth; Wetterwald, Antionette; Wingenfeld, Carsten; Rothen-Rutishauser, Barbara; Gimmi, Claude D. (2002).
415:"Immunization with HIV-1 gp41 subunit virosomes induces mucosal antibodies protecting nonhuman primates against vaginal SHIV challenges"
315:
48:
because it won't cause infection and the viral structure allows the virosome to recognize specific components of its target cells.
36:
130:
bilayer membrane. They have a typical mean diameter of 150 nm. Essentially, virosomes represent reconstituted empty
45:
239:"Virosome, a hybrid vehicle for efficient and safe drug delivery and its emerging application in cancer treatment"
455:
87:
508:
467:
436:
394:
311:
299:
293:
268:
260:
210:
426:
386:
303:
250:
200:
139:
91:
237:
Liu, Hanqing; Tu, Zhigang; Feng, Fan; Shi, Haifeng; Chen, Keping; Xu, Ximing (2015-06-01).
131:
352:
39:
incorporating virus derived proteins to allow the virosomes to fuse with target cells.
502:
288:
123:
119:
74:
70:
135:
127:
115:
102:
62:
57:
32:
390:
431:
414:
189:"A Multipurpose and Novel Carrier for Drug Delivery and Targeting - Virosomes"
161:
They were used as a drug carrier mechanism for experimental cancer therapies.
488:
264:
214:
35:
consisting of unilamellar phospholipid membrane (either a mono- or bi-layer)
493:
471:
440:
398:
307:
272:
255:
238:
205:
188:
111:
66:
19:
456:"Targeting her-2/neu with antirat Neu virosomes for cancer therapy"
155:
143:
101:
40:
187:
Kapoor, D.; Vyas, R. B.; Lad, C.; Patel, M. (2013-09-14).
56:
Virosomes are vehicles that have a spherical shape with a
287:
114:, virosomes contain functional viral envelope
8:
430:
254:
204:
193:Journal of Drug Delivery and Therapeutics
18:
179:
7:
232:
230:
228:
226:
224:
154:They are also being considered for
106:Components of an influenza virosome
33:drug or vaccine delivery mechanism
16:Drug or vaccine delivery mechanism
14:
341:from the original on 2009-02-06.
1:
391:10.1016/j.vaccine.2005.04.026
432:10.1016/j.immuni.2011.01.015
525:
331:"Hemagglutinin Definition"
295:Encyclopedia of Immunology
134:envelopes, devoid of the
126:(NA) intercalated in the
58:phospholipid mono/bilayer
494:"Virosome based vaccine"
92:humoral immune responses
23:Components of a Virosome
165:Benefits and challenges
150:Non-influenza virosomes
308:10.1006/rwei.1999.0055
286:Sela, Michael (1998),
256:10.1515/acph-2015-0019
206:10.22270/jddt.v3i5.627
107:
24:
489:"What are virosomes?"
298:, Elsevier, pp.
105:
81:Virosome applications
22:
98:Influenza virosomes
52:Virosomes structure
243:Acta Pharmaceutica
158:vaccine research.
118:: influenza virus
108:
25:
357:meshb.nlm.nih.gov
516:
476:
475:
451:
445:
444:
434:
409:
403:
402:
373:
367:
366:
364:
363:
349:
343:
342:
327:
321:
320:
291:
283:
277:
276:
258:
234:
219:
218:
208:
184:
140:genetic material
524:
523:
519:
518:
517:
515:
514:
513:
499:
498:
485:
480:
479:
460:Cancer Research
453:
452:
448:
411:
410:
406:
376:
374:
370:
361:
359:
351:
350:
346:
329:
328:
324:
318:
285:
284:
280:
236:
235:
222:
186:
185:
181:
176:
167:
152:
132:influenza virus
110:In contrast to
100:
83:
54:
17:
12:
11:
5:
522:
520:
512:
511:
501:
500:
497:
496:
491:
484:
483:External links
481:
478:
477:
466:(2): 437–444.
446:
425:(2): 269–280.
404:
368:
353:"MeSH Browser"
344:
322:
316:
278:
249:(2): 105–116.
220:
199:(5): 143–147.
178:
177:
175:
172:
166:
163:
151:
148:
142:of the source
138:including the
99:
96:
82:
79:
71:haemagglutinin
53:
50:
15:
13:
10:
9:
6:
4:
3:
2:
521:
510:
507:
506:
504:
495:
492:
490:
487:
486:
482:
473:
469:
465:
461:
457:
450:
447:
442:
438:
433:
428:
424:
420:
416:
408:
405:
400:
396:
392:
388:
384:
380:
372:
369:
358:
354:
348:
345:
340:
336:
332:
326:
323:
319:
317:9780122267659
313:
309:
305:
301:
297:
296:
290:
282:
279:
274:
270:
266:
262:
257:
252:
248:
244:
240:
233:
231:
229:
227:
225:
221:
216:
212:
207:
202:
198:
194:
190:
183:
180:
173:
171:
164:
162:
159:
157:
149:
147:
145:
141:
137:
133:
129:
125:
124:neuraminidase
121:
120:hemagglutinin
117:
116:glycoproteins
113:
104:
97:
95:
93:
89:
88:cell mediated
80:
78:
76:
75:neuraminidase
72:
68:
64:
63:glycoproteins
59:
51:
49:
47:
42:
38:
34:
30:
21:
463:
459:
449:
422:
418:
407:
382:
378:
371:
360:. Retrieved
356:
347:
335:Merck source
334:
325:
294:
281:
246:
242:
196:
192:
182:
168:
160:
153:
136:nucleocapsid
128:phospholipid
109:
84:
55:
28:
26:
509:Vaccination
385:: S26–38.
362:2019-01-03
289:"Antigens"
174:References
265:1846-9558
215:2250-1177
122:(HA) and
112:liposomes
503:Category
472:11809693
441:21315623
419:Immunity
399:16026906
339:Archived
273:26011928
29:virosome
379:Vaccine
300:201–207
67:antigen
41:Viruses
37:vesicle
470:
439:
397:
314:
271:
263:
213:
73:, and
46:vector
156:HIV-1
144:virus
31:is a
468:PMID
437:PMID
395:PMID
312:ISBN
269:PMID
261:ISSN
211:ISSN
90:and
427:doi
387:doi
304:doi
251:doi
201:doi
505::
464:62
462:.
458:.
435:.
423:34
421:.
417:.
393:.
383:23
381:.
355:.
337:.
333:.
310:,
302:,
292:,
267:.
259:.
247:65
245:.
241:.
223:^
209:.
195:.
191:.
146:.
69:,
27:A
474:.
443:.
429::
401:.
389::
375:h
365:.
306::
275:.
253::
217:.
203::
197:3
Text is available under the Creative Commons Attribution-ShareAlike License. Additional terms may apply.