HIV coreceptor and chemokine ligand gene expression in the male urethra and female cervix

被引:17
作者
McClure, CP
Tighe, PJ
Robins, RA
Bansal, D
Bowman, CA
Kingston, M
Ball, JK
机构
[1] Univ Nottingham, Queens Med Ctr, Div Microbiol & Infect Dis, Inst Infect Immun & Inflammat, Nottingham NG7 2UH, England
[2] Univ Nottingham, Div Mol & Clin Immunol, Inst Infect Immun & Inflammat, Nottingham NG7 2RD, England
[3] City Hosp Nottingham, Dept Genitourinary Med, Nottingham, England
关键词
HIV; heterosexual transmission; chemokine receptor; chemokines; mRNA expression; RT-PCR; genital tract;
D O I
10.1097/01.aids.0000180096.50393.96
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: Isolates with a tropism for the coreceptor CCR5 are the predominant viral strain transmitted following heterosexual transmission. We have investigated coreceptor expression levels within male and female genital epithelia to assess whether selective transmission can be explained by elevated CCR5 expression within the genital epithelia perse. Design: Individuals attending a local genitourinary medicine unit were recruited, and samples of genital epithelia obtained using either a cytobrush (females) or urethral swab (males). Expression of coreceptor and cell marker mRNAs was then determined by reverse transcription (RT)-PCR. Methods: RNA was recovered from the epithelial cell samples then used as templates in competitive quantitative RT-PCR to measure mRNA expression of key chemokines, coreceptors and cell-type markers in the epithelial cell samples. Cell-surface coreceptor expression was also assessed in a sample of patients using fluorescent cell staining. Results: CXCR4 and CCR3 coreceptors were expressed at significantly higher levels than CCR5 within the female endo- and ectocervix and distal end of the male urethra. Increased levels of cell surface expressed CXCR4 compared to CCR5 was confirmed in samples obtained from the female genital tract by FACS analysis. Conclusions: The selective transmission of CCR5-tropic viral variants is unlikely to result simply from differential coreceptor abundance at the genital epithelia. (c) 2005 Lippincott Williams & Wilkins.
引用
收藏
页码:1257 / 1265
页数:9
相关论文
共 58 条
[21]   2 INFLAMMATORY MEDIATOR CYTOKINE GENES ARE CLOSELY LINKED AND VARIABLY AMPLIFIED ON CHROMOSOME-17Q [J].
IRVING, SG ;
ZIPFEL, PF ;
BALKE, J ;
MCBRIDE, OW ;
MORTON, CC ;
BURD, PR ;
SIEBENLIST, U ;
KELLY, K .
NUCLEIC ACIDS RESEARCH, 1990, 18 (11) :3261-3270
[22]   Cervical human immunodeficiency virus type 1 shedding is associated with genital β-chemokine secretion [J].
Iversen, AKN ;
Fugger, L ;
Eugen-Olsen, J ;
Balslev, U ;
Jensen, T ;
Wahl, S ;
Gerstoft, J ;
Mullins, JI ;
Skinhoj, P .
JOURNAL OF INFECTIOUS DISEASES, 1998, 178 (05) :1334-1342
[23]   Increase in endocervical CD4 lymphocytes among women with nonulcerative sexually transmitted diseases [J].
Levine, WC ;
Pope, V ;
Bhoomkar, A ;
Tambe, P ;
Lewis, JS ;
Zaidi, AA ;
Farshy, CE ;
Mitchell, S ;
Talkington, DF .
JOURNAL OF INFECTIOUS DISEASES, 1998, 177 (01) :167-174
[24]   The number and distribution of immune cells in the cervicovaginal mucosa remain constant throughout the menstrual cycle of rhesus macaques [J].
Ma, ZM ;
Lü, FX ;
Torten, M ;
Miller, CJ .
CLINICAL IMMUNOLOGY, 2001, 100 (02) :240-249
[25]   A polymerase chain reaction method for the amplification of full-length envelope genes of HIV-1 from DNA samples containing single molecules of HIV-1 provirus [J].
McClure, P ;
Curran, R ;
Boneham, S ;
Ball, JK .
JOURNAL OF VIROLOGICAL METHODS, 2000, 88 (01) :73-80
[26]   Target cells in vaginal HIV transmission [J].
Miller, CJ ;
Shattock, RJ .
MICROBES AND INFECTION, 2003, 5 (01) :59-67
[27]  
MILLER CJ, 1992, J MED PRIMATOL, V21, P64
[28]   The distribution of immunocompetent cells in the genital tract of HIV-positive women [J].
Olaitan, A ;
Johnson, MA ;
MacLean, A ;
Poulter, LW .
AIDS, 1996, 10 (07) :759-764
[29]   QUANTITATIVE TITRATION OF NUCLEIC-ACIDS BY ENZYMATIC AMPLIFICATION REACTIONS RUN TO SATURATION [J].
PANNETIER, C ;
DELASSUS, S ;
DARCHE, S ;
SAUCIER, C ;
KOURILSKY, P .
NUCLEIC ACIDS RESEARCH, 1993, 21 (03) :577-583
[30]  
PARAISO MFR, 1994, OBSTET GYNECOL, V84, P539