Current progress on development of respiratory syncytial virus vaccine

被引:23
作者
Chang, Jun [1 ,2 ]
机构
[1] Ewha Womans Univ, Coll Pharm, Seoul 120750, South Korea
[2] Ewha Womans Univ, Div Life & Pharmaceut Sci, Seoul 120750, South Korea
关键词
Pathogenesis; Protection; Respiratory syncytial virus; Vaccine; Vaccine strategy; FORMALIN-INACTIVATED RSV; ENHANCED PULMONARY HISTOPATHOLOGY; ATTACHMENT G GLYCOPROTEIN; T-CELL RESPONSES; COTTON RATS; BALB/C MICE; F-PROTEIN; INTRANASAL IMMUNIZATION; SEROPOSITIVE CHILDREN; MONOCLONAL-ANTIBODIES;
D O I
10.5483/BMBRep.2011.44.4.232
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Human respiratory syncytial virus (HRSV) is a major cause of upper and lower respiratory tract illness in infants and young children worldwide. Despite its importance as a respiratory pathogen, there is currently no licensed vaccine for prophylaxis of HRSV infection. There are several hurdles complicating the development of a RSV vaccine: 1) incomplete immunity to natural RSV infection leading to frequent re-infection, 2) immature immune system and maternal antibodies of newborn infants who are the primary subject population, and 3) imbalanced Th2-biased immune responses to certain vaccine candidates leading to exacerbated pulmonary disease. After the failure of an initial trial featuring formalin-inactivated virus as a RSV vaccine, more careful and deliberate efforts have been made towards the development of safe and effective RSV vaccines without vaccine-enhanced disease. A wide array of RSV vaccine strategies is being developed, including live-attenuated viruses, protein subunit-based, and vector-based candidates. Though licensed vaccines remain to be developed, our great efforts will lead us to reach the goal of attaining safe and effective RSV vaccines in the near future. [BMB reports 2011; 44(4): 232-237]
引用
收藏
页码:232 / 237
页数:6
相关论文
共 58 条
[1]  
ALWAN WH, 1992, CLIN EXP IMMUNOL, V88, P527
[2]   Complete protection of mice from respiratory syncytial virus infection following mucosal delivery of synthetic peptide vaccines [J].
Bastien, N ;
Trudel, M ;
Simard, C .
VACCINE, 1999, 17 (7-8) :832-836
[3]   Respiratory syncytial virus infection of gene gun vaccinated mice induces Th2-driven pulmonary eosinophilia even in the absence of sensitisation to the fusion (F) or attachment (G) protein [J].
Bembridge, GP ;
Rodriguez, N ;
Garcia-Beato, R ;
Nicolson, C ;
Melero, JA ;
Taylor, G .
VACCINE, 2000, 19 (9-10) :1038-1046
[4]   The Secreted Form of Respiratory Syncytial Virus G Glycoprotein Helps the Virus Evade Antibody-Mediated Restriction of Replication by Acting as an Antigen Decoy and through Effects on Fc Receptor-Bearing Leukocytes [J].
Bukreyev, Alexander ;
Yang, Lijuan ;
Fricke, Jens ;
Cheng, Lily ;
Ward, Jerrold M. ;
Murphy, Brian R. ;
Collins, Peter L. .
JOURNAL OF VIROLOGY, 2008, 82 (24) :12191-12204
[5]   Partial protection to respiratory syncytial virus (RSV) elicited in mice by intranasal immunization using live staphylococci with surface-displayed RSV-peptides [J].
Cano, F ;
Plotnicky-Gilquin, H ;
Nguyen, TN ;
Liljeqvist, S ;
Samuelson, P ;
Bonnefoy, JY ;
Ståhl, S ;
Robert, A .
VACCINE, 2000, 18 (24) :2743-2752
[6]   Respiratory syncytial virus infection suppresses lung CD8+ T-cell effector activity and peripheral CD8+ T-cell memory in the respiratory tract [J].
Chang, J ;
Braciale, TJ .
NATURE MEDICINE, 2002, 8 (01) :54-60
[7]   RESPIRATORY SYNCYTIAL VIRUS (RSV) F-PROTEIN, G-PROTEIN, M2-PROTEIN (22K), AND N-PROTEINS EACH INDUCE RESISTANCE TO RSV CHALLENGE, BUT RESISTANCE INDUCED BY M2-PROTEINS AND N-PROTEINS IS RELATIVELY SHORT-LIVED [J].
CONNORS, M ;
COLLINS, PL ;
FIRESTONE, CY ;
MURPHY, BR .
JOURNAL OF VIROLOGY, 1991, 65 (03) :1634-1637
[8]   ENHANCED PULMONARY HISTOPATHOLOGY INDUCED BY RESPIRATORY SYNCYTIAL VIRUS (RSV) CHALLENGE OF FORMALIN-INACTIVATED RSV-IMMUNIZED BALB/C MICE IS ABROGATED BY DEPLETION OF INTERLEUKIN-4 (IL-4) AND IL-10 [J].
CONNORS, M ;
GIESE, NA ;
KULKARNI, AB ;
FIRESTONE, CY ;
MORSE, HC ;
MURPHY, BR .
JOURNAL OF VIROLOGY, 1994, 68 (08) :5321-5325
[9]   RESISTANCE TO RESPIRATORY SYNCYTIAL VIRUS (RSV) CHALLENGE INDUCED BY INFECTION WITH A VACCINIA VIRUS RECOMBINANT EXPRESSING THE RSV M2 PROTEIN (VAC-M2) IS MEDIATED BY CD8+ T-CELLS, WHILE THAT INDUCED BY VAC-F OR VAC-G RECOMBINANTS IS MEDIATED BY ANTIBODIES [J].
CONNORS, M ;
KULKARNI, AB ;
COLLINS, PL ;
FIRESTONE, CY ;
HOLMES, KL ;
MORSE, HC ;
MURPHY, BR .
JOURNAL OF VIROLOGY, 1992, 66 (02) :1277-1281
[10]   Passively acquired antibodies suppress humoral but not cell-mediated immunity in mice immunized with live attenuated respiratory syncytial virus vaccines [J].
Crowe, JE ;
Firestone, CY ;
Murphy, BR .
JOURNAL OF IMMUNOLOGY, 2001, 167 (07) :3910-3918