Protection of macaques against vaginal SHIV challenge by systemic or mucosal and systemic vaccinations with HIV-envelope

被引:95
作者
Barnetta, Susan W. [1 ]
Srivastava, Indresh K. [1 ]
Kan, Elaine [1 ]
Zhou, Fengmin [1 ]
Goodsell, Amanda [1 ]
Cristillo, Anthony D. [2 ]
Ferrai, Maria Grazia [2 ]
Weiss, Deborah E. [2 ]
Letvin, Norman L. [3 ]
Montefiori, David [4 ]
Pal, Ranajit
Vajdy, Michael [1 ]
机构
[1] Novartis Vaccines & Diag Inc, Emeryville, CA 94608 USA
[2] Adv Biosci Labs Inc, Kensington, NSW, Australia
[3] Harvard Univ, Sch Med, Beth Israel Med Ctr, Dept Med,Div Viral Pathogenesis, Boston, MA USA
[4] Duke Univ, Med Ctr, Lab AIDS Vaccine Res & Dev, Dept Surg, Durham, NC USA
关键词
CD4+T cells; HIV; mucosal vaccine; rhesus macaque; vaginal challenge;
D O I
10.1097/QAD.0b013e3282f3ca57
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Worldwide, the majority of human immunodeficiency virus (HIV) infections occur by heterosexual transmission. Thus, the development of a vaccine that can prevent intravaginal HIV infection is an important goal of AIDS vaccine research. Objectives: To determine which single or combination of systemic and mucosal routes of immunizations of female rhesus macaques with an HIV-1(SF162) envelope protein vaccine induced protection against intravaginal challenge with SHIV. Design: Female rhesus macaques were immunized with an HIV-1(SF162) envelope protein vaccine administered systemically (intramuscularly), or mucosally (intranasally), or as a sequential combination of both routes. The macaques were then challenged intravaginally with SHIVSF162P4, expressing an envelope that is closely matched (homologous) to the vaccine. Results: Macaques receiving intramuscular immunizations, alone or in combination with intranasal immunizations, were protected from infection, with no detectable plasma viral RNA, provirus, or seroconversion to nonvaccine viral proteins, and better preservation of intestinal CD4+ T cells. Serum neutralizing antibodies against the challenge virus appeared to correlate with protection. Conclusions: The results of this study demonstrate that, in the nonhuman primate model, it is possible for vaccine-elicited immune responses to prevent infection after intravaginal administration of virus. (C) 2008 Wolters Kluwer Health | Lippincott Williams & Wilkins.
引用
收藏
页码:339 / 348
页数:10
相关论文
共 47 条
[1]   New viral vaccines [J].
Arvin, AM ;
Greenberg, HB .
VIROLOGY, 2006, 344 (01) :240-249
[2]   Human neutralizing monoclonal antibodies of the IgG1 subtype protect against mucosal simian-human immunodeficiency virus infection [J].
Baba, TW ;
Liska, V ;
Hofmann-Lehmann, R ;
Vlasak, J ;
Xu, WD ;
Ayehunie, S ;
Cavacini, LA ;
Posner, MR ;
Katinger, H ;
Stiegler, G ;
Bernacky, BJ ;
Rizvi, TA ;
Schmidt, R ;
Hill, LR ;
Keeling, ME ;
Lu, YC ;
Wright, JE ;
Chou, TC ;
Ruprecht, RM .
NATURE MEDICINE, 2000, 6 (02) :200-206
[3]   Seroprevalence and immunization history of selected vaccine preventable diseases in medical students [J].
Baer, G ;
Bonhoeffer, J ;
Schaad, UB ;
Heininger, U .
VACCINE, 2005, 23 (16) :2016-2020
[4]   The ability of an oligomeric human immunodeficiency virus type 1 (HIV-1) envelope antigen to elicit neutralizing antibodies against primary HIV-1 isolates is improved following partial deletion of the second hypervariable region [J].
Barnet, SW ;
Lu, S ;
Srivastava, I ;
Cherpelis, S ;
Gettie, A ;
Blanchard, J ;
Wang, S ;
Mboudjeka, I ;
Leung, L ;
Lian, Y ;
Fong, A ;
Buckner, C ;
Ly, A ;
Hilt, S ;
Ulmer, J ;
Wild, CT ;
Mascola, JR ;
Stamatatos, L .
JOURNAL OF VIROLOGY, 2001, 75 (12) :5526-5540
[5]   Mucosal alloimmunization elicits T-cell proliferation, CC chemokines, CCR5 antibodies and inhibition of simian immunodeficiency virus infectivity [J].
Bergmeier, LA ;
Babaahmady, K ;
Wang, YF ;
Lehner, T .
JOURNAL OF GENERAL VIROLOGY, 2005, 86 :2231-2238
[6]   The role of immunity in protection from mucosal SIV infection in macaques [J].
Bergmeier, LA ;
Wang, Y ;
Lehner, T .
ORAL DISEASES, 2002, 8 :63-68
[7]   Protection of MN-rgp120-immunized chimpanzees from heterologous infection with a primary isolate of human immunodeficiency virus type 1 [J].
Berman, PW ;
Murthy, KK ;
Wrin, T ;
Vennari, JC ;
Cobb, EK ;
Eastman, DJ ;
Champe, M ;
Nakamura, GR ;
Davison, D ;
Powell, MF ;
Bussiere, J ;
Francis, DP ;
Matthews, T ;
Gregory, TJ ;
Obijeski, JF .
JOURNAL OF INFECTIOUS DISEASES, 1996, 173 (01) :52-59
[8]   Control of simian/human immunodeficiency virus viremia and disease progression after IL-2-augmented DNA-modified vaccinia virus Ankara nasal vaccination in nonhuman primates [J].
Bertley, FMN ;
Kozlowski, PA ;
Wang, SW ;
Chappelle, J ;
Patel, J ;
Sonuyi, O ;
Mazzara, G ;
Montefiori, D ;
Carville, A ;
Mansfield, KG ;
Aldovini, A .
JOURNAL OF IMMUNOLOGY, 2004, 172 (06) :3745-3757
[9]   Factors associated with slow disease progression in macaques immunized with an adenovirus-simian immunodeficiency virus (SIV) envelope priming-gp120 boosting regimen and challenged vaginally with SIVmac251 [J].
Buge, SL ;
Murty, L ;
Arora, K ;
Kalyanaraman, VS ;
Markham, PD ;
Richardson, ES ;
Aldrich, K ;
Patterson, LJ ;
Miller, CJ ;
Cheng, SM ;
Robert-Guroff, M .
JOURNAL OF VIROLOGY, 1999, 73 (09) :7430-7440
[10]   Efficacy of a SHIV 89.6 proviral DNA vaccine against mucosal SIVmac239 challenge [J].
Busch, M ;
Abel, K ;
Li, J ;
Piatak, M ;
Lifson, JD ;
Miller, CJ .
VACCINE, 2005, 23 (31) :4036-4047