HIV-1 Superinfection in Women Broadens and Strengthens the Neutralizing Antibody Response

被引:63
作者
Cortez, Valerie [1 ,2 ,3 ]
Odem-Davis, Katherine [3 ]
McClelland, R. Scott [2 ]
Jaoko, Walter [4 ]
Overbaugh, Julie [3 ]
机构
[1] Univ Washington, Mol & Cellular Biol Grad Program, Seattle, WA 98195 USA
[2] Univ Washington, Dept Epidemiol, Seattle, WA 98195 USA
[3] Univ Washington, Fred Hutchinson Canc Res Ctr, Div Human Biol, Seattle, WA 98195 USA
[4] Univ Nairobi, Dept Med Microbiol, Nairobi, Kenya
关键词
IMMUNODEFICIENCY-VIRUS TYPE-1; SUBTYPE-C; HORMONAL CONTRACEPTION; MONOCLONAL-ANTIBODIES; DISEASE PROGRESSION; ENVELOPE VARIANTS; HUMORAL IMMUNITY; RHESUS MACAQUES; VIRAL LOAD; ENV CLONES;
D O I
10.1371/journal.ppat.1002611
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Identifying naturally-occurring neutralizing antibodies (NAb) that are cross-reactive against all global subtypes of HIV-1 is an important step toward the development of a vaccine. Establishing the host and viral determinants for eliciting such broadly NAbs is also critical for immunogen design. NAb breadth has previously been shown to be positively associated with viral diversity. Therefore, we hypothesized that superinfected individuals develop a broad NAb response as a result of increased antigenic stimulation by two distinct viruses. To test this hypothesis, plasma samples from 12 superinfected women each assigned to three singly infected women were tested against a panel of eight viruses representing four different HIV-1 subtypes at matched time points post-superinfection (similar to 5 years post-initial infection). Here we show superinfected individuals develop significantly broader NAb responses post-superinfection when compared to singly infected individuals (RR = 1.68, CI: 1.23-2.30, p = 0.001). This was true even after controlling for NAb breadth developed prior to superinfection, contemporaneous CD4+ T cell count and viral load. Similarly, both unadjusted and adjusted analyses showed significantly greater potency in superinfected cases compared to controls. Notably, two superinfected individuals were able to neutralize variants from four different subtypes at plasma dilutions >1:300, suggesting that their NAbs exhibit elite activity. Cross-subtype breadth was detected within a year of superinfection in both of these individuals, which was within 1.5 years of their initial infection. These data suggest that sequential infections lead to augmentation of the NAb response, a process that may provide insight into potential mechanisms that contribute to the development of antibody breadth. Therefore, a successful vaccination strategy that mimics superinfection may lead to the development of broad NAbs in immunized individuals.
引用
收藏
页数:11
相关论文
共 52 条
[1]   Enhancing exposure of HIV-1 neutralization epitopes through mutations in gp41 [J].
Blish, Catherine A. ;
Nguyen, Minh-An ;
Overbaugh, Julie .
PLOS MEDICINE, 2008, 5 (01) :90-103
[2]   HIV-1 subtype A envelope variants from early in infection have variable sensitivity to neutralization and to inhibitors of viral entry [J].
Blish, Catherine A. ;
Nedellec, Rebecca ;
Mandaliya, Kishorchandra ;
Mosier, Donald E. ;
Overbaugh, Julie .
AIDS, 2007, 21 (06) :693-702
[3]   Cross-Subtype Neutralization Sensitivity despite Monoclonal Antibody Resistance among Early Subtype A, C, and D Envelope Variants of Human Immunodeficiency Virus Type 1 [J].
Blish, Catherine A. ;
Jalalian-Lechak, Zahra ;
Rainwater, Stephanie ;
Nguyen, Minh-An ;
Dogan, Ozge C. ;
Overbaugh, Julie .
JOURNAL OF VIROLOGY, 2009, 83 (15) :7783-7788
[4]   Human Immunodeficiency Virus Type 1 Superinfection Occurs despite Relatively Robust Neutralizing Antibody Responses [J].
Blish, Catherine A. ;
Dogan, Ozge C. ;
Derby, Nina R. ;
Nguyen, Minh-An ;
Chohan, Bhavna ;
Richardson, Barbra A. ;
Overbaugh, Julie .
JOURNAL OF VIROLOGY, 2008, 82 (24) :12094-12103
[5]   TIME-COURSE OF DETECTION OF VIRAL AND SEROLOGIC MARKERS PRECEDING HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 SEROCONVERSION - IMPLICATIONS FOR SCREENING OF BLOOD AND TISSUE DONORS [J].
BUSCH, MP ;
LEE, LLL ;
SATTEN, GA ;
HENRARD, DR ;
FARZADEGAN, H ;
NELSON, KE ;
READ, S ;
DODD, RY ;
PETERSEN, LR .
TRANSFUSION, 1995, 35 (02) :91-97
[6]   ISOLATES OF HUMAN IMMUNODEFICIENCY VIRUS TYPE-1 FROM THE BRAIN MAY CONSTITUTE A SPECIAL GROUP OF THE AIDS VIRUS [J].
CHENGMAYER, C ;
WEISS, C ;
SETO, D ;
LEVY, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (21) :8575-8579
[7]   Evidence for frequent reinfection with human immunodeficiency virus type 1 of a different subtype [J].
Chohan, B ;
Lavreys, L ;
Rainwater, SMJ ;
Overbaugh, J .
JOURNAL OF VIROLOGY, 2005, 79 (16) :10701-10708
[8]  
Chohan BH, 2010, CURR HIV RES, V8, P596, DOI 10.2174/157016210794088218
[9]   Neutralizing antibody responses against autologous and heterologous viruses in acute versus chronic human immunodeficiency virus (HIV) infection: Evidence for a constraint on the ability of HIV to completely evade neutralizing antibody responses [J].
Decks, Steven G. ;
Schweighardt, Becky ;
Wrin, Terri ;
Galovich, Justin ;
Hoh, Rebecca ;
Sinclair, Elizabeth ;
Hunt, Peter ;
McCune, Joseph M. ;
Martin, Jeffrey N. ;
Petropoulos, Christos J. ;
Hecht, Frederick M. .
JOURNAL OF VIROLOGY, 2006, 80 (12) :6155-6164
[10]   Evaluation of performance of the Gen-Probe human immunodeficiency virus type 1 viral load assay using primary subtype A, C, and D isolates from Kenya [J].
Emery, S ;
Bodrug, S ;
Richardson, BA ;
Giachetti, C ;
Bott, MA ;
Panteleeff, D ;
Jagodzinski, LL ;
Michael, NL ;
Nduati, R ;
Bwayo, J ;
Kreiss, JK ;
Overbaugh, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (07) :2688-2695