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. 2010 Jun;176(6):2798-805.
doi: 10.2353/ajpath.2010.090926. Epub 2010 Apr 15.

Abundant expression of HIV target cells and C-type lectin receptors in the foreskin tissue of young Kenyan men

Taha Hirbod  1 , Robert C Bailey, Kawango Agot, Stephen Moses, Jeckoniah Ndinya-Achola, Ruth Murugu, Jan Andersson, Jakob Nilsson, Kristina Broliden
Affiliations

Abundant expression of HIV target cells and C-type lectin receptors in the foreskin tissue of young Kenyan men

Taha Hirbod et al. Am J Pathol. 2010 Jun.

Abstract

A biological explanation for the reduction in HIV-1 (HIV) acquisition after male circumcision may be that removal of the foreskin reduces the number of target cells for HIV. The expression of potential HIV target cells and C-type lectin receptors in foreskin tissue of men at risk of HIV infection were thus analyzed. Thirty-three foreskin tissue samples, stratified by Herpes simplex virus type 2 status, were obtained from a randomized, controlled trial conducted in Kenya. The samples were analyzed by confocal in situ imaging microscopy and mRNA quantification by quantitative RT-qPCR. The presence and location of T cells (CD3(+)CD4(+)), Langerhans cells (CD1a(+)Langerin/CD207(+)), macrophages (CD68(+) or CD14(+)), and submucosal dendritic cells (CD123(+)BDCA-2(+) or CD11c(+)DC-SIGN(+)) were defined. C-type lectin receptor expressing cells were detected in both the epithelium and submucosa, and distinct lymphoid aggregates densely populated with CD3(+)CD4(+) T cells were identified in the submucosa. Although the presence of lymphoid aggregates and mRNA expression of selected markers varied between study subjects, Herpes simplex virus type 2 serostatus was not the major determinant for the detected differences. The detection of abundant and superficially present potential HIV target cells and submucosal lymphoid aggregates in foreskin mucosa from a highly relevant HIV risk group demonstrate a possible anatomical explanation that may contribute to the protective effect of male circumcision on HIV transmission.

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Figures

Figure 1
Figure 1
A: CD144 and (B) Podoplanin were solely visible in the submucosa when using the Fast Red Chromogen (Biocare Medical) due to the presence of dark melanocytes in the epithelium. However, when fluorescently labeled markers were used, both (C) CD144 and (D) Podoplanin were detected also in the epithelium (minimum distance to tissue surface [MDTS]: 111 μm and 55 μm, respectively). Black and white arrowheads indicate positive staining. Scale bars = 75 μm. Results are from one of at least four tissue samples yielding similar results.
Figure 2
Figure 2
A: LCs were defined here as CD1a+ (green) and/or Langerin+ (red), and these markers co-localized on the majority of cells (yellow; I: MDTS: 24 μm). B: CD1a+ (green) LCs within the epithelium frequently expressed CD4 (red; yellow cells: double positive; I: MDTS: 37 μm). C: CD1a+ CD4+ (yellow) LCs were also present deep within the submucosa (I: MDTS: 359 μm). D: CD1a+ (red) LCs expressed CD11c (green), and double positive (yellow) cells were found both within the epithelium (I: MDTS: 45 μm) and the submucosa (II: MDTS: 226 μm). E: CD1a+ (green) LCs expressing DC-LAMP (red) were solely present in the submucosal compartment (I: magnification of double positive cell). F: Macrophages were defined here as CD68+ (red) and/or CD14+ (green) cells. Double positive cells (yellow) were rare and located further from the tissue surface as compared with single positive CD68 cells (MDTS I: 248 μm and II: 63 μm). CD68+ (green) cells expressed (G) MR (red; I: MDTS: 198 μm), and (H) CD68+DC-SIGN (yellow) cells were also present, although less frequent (I: MDTS: 54 μm). CD4 (green) was present on submucosal CD11c+ (red) cells (I). CD11c+CD68+ (yellow) cells were frequent in the submucosa (J), whereas CD11c+ (green) cells did not express CD14 (red; K). CD11c+ (green) cells co-localized (yellow) with the CLRs (red): (L) Langerin, (M) MR, and (N) DC-SIGN. O: The pDCs specific marker BDCA-2 was rarely present in the foreskin tissue, when present BDCA-2 always co-localized with CD123+ (red) cells. The pDCs markers used here did not co-express any of the other investigated markers with one exception; (P) CD123+CD4+ (yellow) cells were detected in the submucosal compartment. White arrowheads indicate positive staining. Scale bars = 75 μm. Results are from one of at least four tissue samples yielding similar results.
Figure 3
Figure 3
A: CD4+ (green) and CD3+ (red) frequently co-localized (yellow) within the submucosa of the human foreskin (0.02 cells/100 μm2 tissue). B: The CD4+ cells were observed both within the epithelium (I: MDTS: 92 μm) and deep in the submucosa (II: MDTS: 609 μm). A vast number of CD4+ cells were also detected within lymphoid aggregates, which were present below the basal membrane (III: MDTS: 231 μm; IV: area 10,587 μm2). White arrowheads indicate positive staining. Scale bars = 75 μm. Results are from one of at least four tissue samples yielding similar results. C: Measurements of (I) distance of cell body to tissue surface; (II) epithelial thickness; and (III) thickness of keratin layer were performed on five randomly selected HSV-2 seronegative (HSV-2−) individuals and five randomly selected HSV-2 seropositive (HSV-2+) individuals. All measurements were performed in approximately 5 × 105 μm2 tissue within 700 μm from the tissue surface. Results are presented in D. No differences were detected between HSV-2− and HSV-2+ individuals regarding distance of CD3+ (red bars) or HLA-DR+ (green bars) cells to tissue surface; median (range) in micrometers were as follows: 238 (43 to 683) vs. 238 (65 to 664) and 207 (51 to 508) vs. 189 (59 to 460), respectively. Neither were differences in epithelial thickness (yellow bars) or thickness of keratin layer (blue bars) detected; median (range) in micrometers were as follows: 85 (42 to 232) vs. 88 (38 to 192) and 22 (10 to 42) vs. 23 (13 to 31), respectively. Bars show the medians and error bars the range.
Figure 4
Figure 4
Expression of CD3, CD4, HLA-DR, Langerin/CD207, MR/CD206, DC-SIGN/CD209, CD68, CD11c, CD1a, CD123, BDCA-2, and DC-LAMP mRNA was measured by quantitative PCR. Lines and bars depict geometric mean with 95% confidence interval (asterisk) and boxes indicate statistical significant differences in expression between HSV-2 seropositive individuals (HSV-2+) and HSV-2 seronegative individuals (HSV-2−; statistical test: Mann-Whitney). HSV-2+ individuals had significantly higher levels of MR/CD206 (P = 0.046), CD14 (P = 0.046), and CD123 (P = 0.0002) in their foreskin.
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