Improved health and survival of FIV-infected cats is associated with the presence of autoantibodies to the primary receptor, CD134

被引:14
作者
Grant, Chris K. [2 ]
Fink, Elizabeth A. [1 ]
Sundstrom, Magnus [1 ]
Torbett, Bruce E. [3 ]
Elder, John H. [1 ]
机构
[1] Scripps Res Inst, Dept Immunol & Microbiol Sci, La Jolla, CA 92037 USA
[2] Custom Monoclonals Int, W Sacramento, CA 95691 USA
[3] Scripps Res Inst, Dept Mol & Expt Med, La Jolla, CA 92037 USA
基金
美国国家卫生研究院;
关键词
antireceptor antibody; autoantibody; FIV; lentivirus; virus neutralization; FELINE-IMMUNODEFICIENCY-VIRUS; LYMPH-NODES; ANTIIDIOTYPIC ANTIBODIES; ANTI-CD4; AUTOANTIBODIES; MONOCLONAL-ANTIBODIES; SURFACE GLYCOPROTEIN; TRANSMISSION; BINDING; RECOMBINANT; DISEASE;
D O I
10.1073/pnas.0911307106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We analyzed antibody responses in sera from feline immunodeficiency virus (FIV)-infected and uninfected cats. A strong antiviral response to the viral surface glycoprotein (SU) was noted in both natural and experimental infections. In addition, 143 of 226 FIV-infected animals (63%) also expressed antibodies to the primary binding receptor, CD134, whereas cats infected with other feline RNA viruses, including calicivirus, coronavirus, herpesvirus, and feline leukemia virus, did not. Both affinity-purified anti-CD134 and anti-SU antibodies blocked FIV infection ex vivo. FACS analyses revealed that the anti-CD134 antibodies bound to a cryptic epitope on the receptor that was only exposed when SU bound to CD134. Anti-CD134 binding caused displacement of SU from the surface of the cell and inhibition of infection. The presence of antibodies to CD134 correlated with lower virus loads and a better overall health status in FIV+ cats, whereas anti-SU antibodies were present independent of health status. The findings are consistent with a role for antireceptor antibodies in protection from virus spread and disease progression.
引用
收藏
页码:19980 / 19985
页数:6
相关论文
共 45 条
[1]   EARLY STAGES OF FELINE IMMUNODEFICIENCY VIRUS-INFECTION IN LYMPH-NODES AND SPLEEN [J].
BACH, JM ;
HURTREL, M ;
CHAKRABARTI, L ;
GANIERE, JP ;
MONTAGNIER, L ;
HURTREL, B .
AIDS RESEARCH AND HUMAN RETROVIRUSES, 1994, 10 (12) :1731-1738
[2]   Induction of murine mucosal CCR5-reactive antibodies as an anti-human immunodeficiency virus strategy [J].
Barassi, C ;
Soprana, E ;
Pastori, C ;
Longhi, R ;
Buratti, E ;
Lillo, F ;
Marenzi, C ;
Lazzarin, A ;
Siccardi, AG ;
Lopalco, L .
JOURNAL OF VIROLOGY, 2005, 79 (11) :6848-6858
[3]   PRIMARY STAGE OF FELINE IMMUNODEFICIENCY VIRUS-INFECTION - VIRAL DISSEMINATION AND CELLULAR TARGETS [J].
BEEBE, AM ;
DUA, N ;
FAITH, TG ;
MOORE, PF ;
PEDERSEN, NC ;
DANDEKAR, S .
JOURNAL OF VIROLOGY, 1994, 68 (05) :3080-3091
[4]   CLINICAL AND PATHOLOGICAL FINDINGS IN FELINE IMMUNODEFICIENCY VIRUS EXPERIMENTAL-INFECTION [J].
CALLANAN, JJ ;
THOMPSON, H ;
TOTH, SR ;
ONEIL, B ;
LAWRENCE, CE ;
WILLETT, B ;
JARRETT, O .
VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 1992, 35 (1-2) :3-13
[5]  
CALLANAN JJ, 1993, MORPHOLOGIC CHARACTE, P115
[6]   DETECTION OF ANTI-CD4 AUTOANTIBODIES IN THE SERA OF HIV-INFECTED PATIENTS USING RECOMBINANT SOLUBLE CD4 MOLECULES [J].
CHAMS, V ;
JOUAULT, T ;
FENOUILLET, E ;
GLUCKMAN, JC ;
KLATZMANN, D .
AIDS, 1988, 2 (05) :353-361
[7]   ANTIIDIOTYPIC ANTIBODIES TO HUMAN ANTI-GP120 ANTIBODIES BIND RECOMBINANT AND CELLULAR HUMAN CD4 [J].
CORRE, JP ;
FEVRIER, M ;
CHAMARET, S ;
THEZE, J ;
ZOUALI, M .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1991, 21 (03) :743-751
[8]   Sequential CD134-CXCR4 interactions in feline immunodeficiency virus (FIV): Soluble CD134 activates FIV Env for CXCR4-dependent entry and reveals a cryptic neutralization epitope [J].
de Parseval, A ;
Grant, CK ;
Sastry, KJ ;
Elder, JH .
JOURNAL OF VIROLOGY, 2006, 80 (06) :3088-3091
[9]   Structural mapping of CD134 residues critical for interaction with feline immunodeficiency virus [J].
de Parseval, A ;
Chatterji, U ;
Morris, G ;
Sun, PQ ;
Olson, AJ ;
Elder, JH .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2005, 12 (01) :60-66
[10]   Feline immunodeficiency virus targets activated CD4+ T cells by using CD134 as a binding receptor [J].
de Parseval, A ;
Chatterji, U ;
Sun, PQ ;
Elder, JH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (35) :13044-13049