Germinal centre CD4+ T cells are an important site of HIV replication in vivo

被引:108
作者
Hufert, FT
vanLunzen, J
Janossy, G
Bertram, S
Schmitz, J
Haller, O
Racz, P
vonLaer, D
机构
[1] BERNHARD NOCHT INST TROP MED,DEPT CLIN,HAMBURG,GERMANY
[2] ROYAL FREE HOSP,SCH MED,DEPT CLIN IMMUNOL,LONDON,ENGLAND
[3] HARVARD UNIV,BETH ISRAEL HOSP,DIV VIRAL PATHOGENESIS,SCH MED,BOSTON,MA 02215
[4] BERNHARD NOCHT INST TROP MED,DEPT PATHOL,HAMBURG,GERMANY
关键词
HIV-1; lymphadenopathy; lymphoid tissue; germinal centre; viral load; HIV replication; flow cytometry; CD4; CD57;
D O I
10.1097/00002030-199707000-00003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Objective: CD4+ T cells are the main target for HIV. However, the highest HIV antigen concentration in infected subjects accumulates on the cell surface of follicular dendritic cells in the germinal centres of the lymphoid tissue. Germinal centres contain a T-helper cell subset which expresses CD57 molecules. Here we analysed virus replication and viral load in CD57+CD4+ germinal centre T cells and in the CD4+ T cells found mostly outside germinal centres (CD57-CD4+). Methods: Peripheral blood mononuclear cells and lymph-node cells were prepared, stained for CD4 and CD57 and purified by FAGS. Defined cell numbers of CD4+CD57+ cells and CD4+CD57- cells were sorted directly into polymerase chain reaction (PCR) tubes by FACS, equipped with an automated cell deposition unit and analysed by PCR to detect proviral DNA. Based on Poisson distribution, the expected level of infection was calculated. Viral replication was determined by amplifying double-spliced, single-spliced, and full-length transcripts of HIV using serially diluted cDNA of the FACS-sorted cells. Results: An up to 10-fold higher frequency of infected cells was found in the CD57+CD4+ germinal centre T cells compared with CD57-CD4+ T cells. Furthermore, active viral replication was detected almost exclusively in the CD57+CD4+ T cells. Conclusions: The CD57+CD4+ germinal centre T cells are one of the sites of HIV infection and replication that may play a pivotal role in the pathogenesis of HIV infection.
引用
收藏
页码:849 / 857
页数:9
相关论文
共 51 条
[1]
DETECTION OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 PROVIRUS IN MONONUCLEAR-CELLS BY INSITU POLYMERASE CHAIN-REACTION [J].
BAGASRA, O ;
HAUPTMAN, SP ;
LISCHNER, HW ;
SACHS, M ;
POMERANTZ, RJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1992, 326 (21) :1385-1391
[2]
BERTRAM S, 1995, BIOTECHNIQUES, V19, P616
[3]
BIBERFELD P, 1985, CANCER RES, V45, P4665
[4]
LYMPHOCYTE-ACTIVATION IN HIV-1 INFECTION .2. FUNCTIONAL DEFECTS OF CD28- T-CELLS [J].
BORTHWICK, NJ ;
BOFILL, M ;
GOMBERT, WM ;
AKBAR, AN ;
MEDINA, E ;
SAGAWA, K ;
LIPMAN, MC ;
JOHNSON, MA ;
JANOSSY, G .
AIDS, 1994, 8 (04) :431-441
[5]
GERMINAL CENTER T-CELLS ARE DISTINCT HELPER-INDUCER T-CELLS [J].
BOWEN, MB ;
BUTCH, AW ;
PARVIN, CA ;
LEVINE, A ;
NAHM, MH .
HUMAN IMMUNOLOGY, 1991, 31 (01) :67-75
[6]
[Anonymous], 1992, MMWR Recomm Rep, V41, P1
[7]
CHALIFOUX LV, 1984, LAB INVEST, V51, P22
[8]
IMMUNOENZYMATIC LABELING OF MONOCLONAL-ANTIBODIES USING IMMUNE-COMPLEXES OF ALKALINE-PHOSPHATASE AND MONOCLONAL ANTI-ALKALINE PHOSPHATASE (APAAP COMPLEXES) [J].
CORDELL, JL ;
FALINI, B ;
ERBER, WN ;
GHOSH, AK ;
ABDULAZIZ, Z ;
MACDONALD, S ;
PULFORD, KAF ;
STEIN, H ;
MASON, DY .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1984, 32 (02) :219-229
[9]
THE SIMIAN IMMUNODEFICIENCY VIRUSES [J].
DESROSIERS, RC .
ANNUAL REVIEW OF IMMUNOLOGY, 1990, 8 :557-578
[10]
MASSIVE COVERT INFECTION OF HELPER T-LYMPHOCYTES AND MACROPHAGES BY HIV DURING THE INCUBATION PERIOD OF AIDS [J].
EMBRETSON, J ;
ZUPANCIC, M ;
RIBAS, JL ;
BURKE, A ;
RACZ, P ;
TENNERRACZ, K ;
HAASE, AT .
NATURE, 1993, 362 (6418) :359-362