Impairment of T Cell Immunity by the Respiratory Syncytial Virus: Targeting Virulence Mechanisms for Therapy and Prophylaxis

被引:22
作者
Gonzalez, P. A. [1 ]
Bueno, S. M. [1 ]
Riedel, C. A. [1 ,3 ,4 ]
Kalergis, A. M. [1 ,2 ]
机构
[1] Pontificia Univ Catolica Chile, Fac Ciencias Biol, Dept Mol Genet & Microbiol, Santiago 8331010, Chile
[2] Pontificia Univ Catolica Chile, Fac Med, Dept Reumatol, Santiago 8331010, Chile
[3] Univ Andres Bello, Fac Ciencias Biol, Dept Ciencias Biol, Lab Biol Celular & Farmacol, Santiago, Chile
[4] Univ Andres Bello, Fac Med, Santiago, Chile
关键词
Dendritic cells; T cell immunity; virulence factors; immune evasion; recombinant bacteria; vaccines; PLASMACYTOID DENDRITIC CELLS; NATURAL-KILLER-CELLS; PULMONARY EOSINOPHILIA; FUSION PROTEIN; ANTIGEN PRESENTATION; G-GLYCOPROTEIN; INTRANASAL IMMUNIZATION; GENETIC SUSCEPTIBILITY; INHIBITS MATURATION; PROTECTIVE IMMUNITY;
D O I
10.2174/092986709789760724
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
Worldwide, respiratory syncytial virus (RSV) causes severe bronchiolitis and pneumonia in children, the elderly and immuno-compromised individuals. Moreover, RSV is the mayor cause of infant hospitalization due to lower respiratory infection, regardless socioeconomic status. Accumulating data support the notion that immune responses elicited against naturally acquired RSV infections are non-lasting and inappropriate for efficient virus clearance. Although there is consensus over the capacity of RSV to impair the development of an effective and protective adaptive immune response, very little is known about specific viral determinants involved in these processes as well as the molecular mechanisms developed by this virus to inhibit T cell function. Recent studies have provided evidence supporting an important role for dendritic cells in RSV-induced suppression of immunity. Although recognized for over 50 years as an important respiratory pathogen and healthcare problem, to date there are no available vaccines against this virus, which highlights the complexity of RSV-induced immunopathology. The development of new prophylactic and therapeutic tools against RSV requires the unveiling of molecular mechanisms and virulence factors responsible for the pathogenesis caused by this virus. In this review, we discuss recent findings describing virulence mechanisms evolved by RSV to negatively modulate the adaptive immune response in the host. Furthermore, novel strategies aimed to induce efficient T cell immunity against RSV are reviewed.
引用
收藏
页码:4609 / 4625
页数:17
相关论文
共 249 条
[51]   Age at first viral infection determines the pattern of T cell-mediated disease during reinfection in adulthood [J].
Culley, FJ ;
Pollott, J ;
Openshaw, PJM .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 196 (10) :1381-1386
[52]   Intranasal proteosome-based respiratory syncytial virus (RSV) vaccines protect BALB/c mice against challenge without eosinophilia or enhanced pathology [J].
Cyr, Sonya L. ;
Jones, Taff ;
Stoica-Popescu, Ioana ;
Brewer, Angela ;
Chabot, Sophie ;
Lussier, Michelle ;
Burt, David ;
Ward, Brian J. .
VACCINE, 2007, 25 (29) :5378-5389
[53]   The enhancement or prevention of airway hyperresponsiveness during reinfection with respiratory syncytial virus is critically dependent on the age at first infection and IL-13 production [J].
Dakhama, A ;
Park, JW ;
Taube, C ;
Joetham, A ;
Balhorn, A ;
Miyahara, N ;
Takeda, K ;
Gelfand, EW .
JOURNAL OF IMMUNOLOGY, 2005, 175 (03) :1876-1883
[54]   The role of virus-specific immunoglobulin E in airway hyperresponsiveness [J].
Dakhama, A ;
Park, JW ;
Taube, C ;
Chayama, K ;
Balhorn, A ;
Joetham, A ;
Wei, XD ;
Fan, RH ;
Swasey, C ;
Miyahara, N ;
Kodama, T ;
Alvarez, A ;
Takeda, K ;
Gelfand, EW .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2004, 170 (09) :952-959
[55]   Virus-specific IgE enhances airway responsiveness on reinfection with respiratory syncytial virus in newborn mice [J].
Dakhama, Azzeddine ;
Lee, Young-Mok ;
Ohnishi, Hiroshi ;
Jing, Xia ;
Balhorn, Annette ;
Takeda, Katsuyuki ;
Gelfand, Erwin W. .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2009, 123 (01) :138-145
[56]   Respiratory syncytial virus infection of monocyte-derived dendritic cells decreases their capacity to activate CD4 T cells [J].
de Graaff, PAA ;
de Jong, EC ;
van Capel, TM ;
van Dijk, MEA ;
Roholl, PJM ;
Boes, J ;
Luytjes, W ;
Kimpen, JLL ;
van Bleek, GM .
JOURNAL OF IMMUNOLOGY, 2005, 175 (09) :5904-5911
[57]   Microbial compounds selectively induce Th1 cell-promoting or Th2 cell-promoting dendritic cells in vitro with diverse Th cell-polarizing signals [J].
de Jong, EC ;
Vieira, PL ;
Kalinski, P ;
Schuitemaker, JHN ;
Tanaka, Y ;
Wierenga, EA ;
Yazdanbakhsh, M ;
Kapsenberg, ML .
JOURNAL OF IMMUNOLOGY, 2002, 168 (04) :1704-1709
[58]   Vaccination of infant macaques with a recombinant modified vaccinia virus Ankara expressing the respiratory syncytial virus F and G genes does not predispose for immunopathology [J].
de Waal, L ;
Wyatt, LS ;
Yüksel, S ;
van Amerongen, G ;
Moss, B ;
Niesters, HGM ;
Osterhaus, ADME ;
de Swart, RL .
VACCINE, 2004, 22 (08) :923-926
[59]   Evaluation of recombinant BCG expressing rotavirus VP6 as an anti-rotavirus vaccine [J].
Dennehy, Maureen ;
Bourn, William ;
Steele, Duncan ;
Williamson, Anna-Lise .
VACCINE, 2007, 25 (18) :3646-3657
[60]   Immunological synapses are versatile structures enabling selective T cell polarization [J].
Depoil, D ;
Zaru, R ;
Guiraud, M ;
Chauveau, A ;
Harriague, J ;
Bismuth, G ;
Utzny, C ;
Müller, S ;
Valitutti, S .
IMMUNITY, 2005, 22 (02) :185-194