Longitudinal Antibody Responses in People Who Inject Drugs Infected With Similar Human Immunodeficiency Virus Strains

被引:2
|
作者
Redd, Andrew D. [1 ,2 ]
Doria-Rose, Nicole A. [3 ]
Weiner, Joshua A. [4 ]
Nason, Martha [5 ]
Seivers, Matthew [2 ]
Schmidt, Stephen D. [3 ]
Laeyendecker, Oliver [1 ,2 ]
Martens, Craig [6 ]
Bruno, Daniel [6 ]
Keele, Brandon F. [7 ]
Raju, Nagarajan [8 ,9 ,10 ]
Georgiev, Ivelin S. [8 ,9 ,10 ]
Lamers, Susanna L. [11 ]
Astemborski, Jacquie [12 ]
Kirk, Gregory D. [12 ]
Mascola, John R. [3 ]
Ackerman, Margaret E. [4 ]
Mehta, Shruti H. [12 ]
Quinn, Thomas C. [1 ,2 ]
机构
[1] NIAID, Lab Immunoregulat, Div Intramural Res, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USA
[2] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
[3] NIAID, Vaccine Res Ctr, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USA
[4] Dartmouth Coll, Hanover, NH 03755 USA
[5] NIAID, Biostat Res Branch, NIH, 9000 Rockville Pike, Bethesda, MD 20892 USA
[6] NIAID, Genom Unit, Res Technol Branch, Rocky Mt Labs,Div Intramural Res,NIH, Hamilton, MT USA
[7] Frederick Natl Lab Canc Res, AIDS & Canc Virus Program, Frederick, MD USA
[8] Vanderbilt Univ, Med Ctr, Dept Pathol Microbiol & Immunol, Nashville, TN USA
[9] Vanderbilt Univ, Dept Elect Engn & Comp Sci, 221 Kirkland Hall, Nashville, TN 37235 USA
[10] Vanderbilt Vaccine Ctr, Nashville, TN USA
[11] BioInfoExperts, Thibodaux, LA USA
[12] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD USA
来源
JOURNAL OF INFECTIOUS DISEASES | 2020年 / 221卷 / 05期
关键词
HIV; neutralizing antibody; antibody development; people who inject drugs; cluster linkage; FC ARRAY; TYPE-1; EVOLUTION; ENVELOPE; BREADTH; ASSAY;
D O I
10.1093/infdis/jiz503
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. Multiple factors influence the human immunodeficiency virus (HIV) antibody response produced during natural infection, leading to responses that can vary in specificity, strength, and breadth. Methods. People who inject drugs identified as recently infected with HIV (n = 23) were analyzed for clustering of their viral sequences (genetic distance, <2%). Longitudinal antibody responses were identified for neutralizing antibody (Nab) potential, and differences in antibody subclass, specificity, and Fc receptor ligation using pseudovirus entry and multiplexed Fc array assays, respectively. Responses were analyzed for differences between subject groups, defined by similarity in the sequence of the infecting virus. Results. Viral sequences from infected individuals were grouped into 3 distinct clusters with 7 unclustered individuals. Subjects in cluster 1 generally had lower antibody response magnitudes, except for antibodies targeting the V1/V2 region. Subjects in clusters 2 and 3 typically had higher antibody response magnitudes, with the Fv specificity of cluster 2 favoring gp140 recognition. NAb responses differed significantly between clusters for 3 of 18 pseudoviruses examined (P < .05), but there were no differences in overall NAb breadth (P = .62). Discussion. These data demonstrate that individuals infected with similar viral strains can generate partially similar antibody responses, but these do not drastically differ from those in individuals infected with relatively unrelated strains.
引用
收藏
页码:756 / 765
页数:10
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