CELLULAR IMMUNE FACTORS ASSOCIATED WITH MOTHER-TO-INFANT TRANSMISSION OF HIV

被引:109
作者
CLERICI, M
SISON, AV
BERZOFSKY, JA
RAKUSAN, TA
BRANDT, CD
ELLAURIE, M
VILLA, M
COLIE, C
VENZON, DJ
SEVER, JL
SHEARER, GM
机构
[1] NCI,EXPTL IMMUNOL BRANCH,BLDG 10,ROOM 4B-17,BETHESDA,MD 20892
[2] GEORGETOWN UNIV,SCH MED,DEPT OBSTET & GYNECOL,WASHINGTON,DC
[3] NCI,METAB BRANCH,BETHESDA,MD 20892
[4] NCI,CLIN ONCOL PROGRAM,BETHESDA,MD 20892
[5] UNIV MILAN,CATTEDRA IMMUNOL,I-20122 MILAN,ITALY
[6] CHILDRENS NATL MED CTR,WASHINGTON,DC
关键词
HIV; T-LYMPHOCYTES; MOTHER-TO-INFANT TRANSMISSION; SYNTHETIC PEPTIDES; INTERLEUKIN-2; POLYMERASE CHAIN REACTION; VIRAL CULTURES;
D O I
10.1097/00002030-199311000-00004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: To study a possible correlate of protection in mother-to-infant transmission of HIV infection. In particular, to determine whether lack of HIV-specific T-helper (TH) function as indicated by HIV and non-HIV antigen-stimulated interleukin (IL)-2 production of mother and/or newborn peripheral blood leukocytes (PBL) is associated with mother-to-infant transmission of HIV. Methods: PBL from 21 HIV-seropositive pregnant women and 23 cord blood leukocytes (CBL) from their offspring were studied for in vitro TH function by IL-2 production in response to HIV and non-HIV antigens. Polymerase chain reaction (PCR) and viral culture assays were performed to determine HIV infection of the infants. Results: PBL from 10 out of 21 (48%) mothers and from eight out of 23 (35%) CBL samples responded to two or more out of five synthetic gp160 envelope (env) peptides. Three of the 23 (13%) offspring were shown to be HIV-infected by PCR and/or viral culture on follow-up. All three infected infants were from a subset whose CBL did not exhibit env-specific TH immunity. Conclusion: Our results demonstrate that fetal T cells can be primed to HIV env determinants in utero, suggest that HIV-specific TH immunity may be protective in newborns, and provide a possible means for identifying newborns who are at risk for HIV infection.
引用
收藏
页码:1427 / 1433
页数:7
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