Abstract

BackgroundThe burden of HPV-associated premalignant and malignant cervical lesions remains high in HIV+ women even under ART treatment. In order to identify possible underlying pathophysiologic mechanisms, we studied activation and HIV co-receptor expression in cervical T-cell populations in relation to HIV, HPV and cervical lesion status.MethodsCervical cytobrush (n = 468: 253 HIV- and 215 HIV+; 71% on ART) and blood (in a subset of 39 women) was collected from women in Mbeya, Tanzania. Clinical data on HIV and HPV infection, as well as ART status was collected. T cell populations were characterized using multiparametric flow cytometry-based on their expression of markers for cellular activation (HLA-DR), and memory (CD45RO), as well as HIV co-receptors (CCR5, α4β7).ResultsCervical and blood T cells differed significantly, with higher frequencies of T cells expressing CD45RO, as well as the HIV co-receptors CCR5 and α4β7 in the cervical mucosa. The skewed CD4/CD8 T cell ratio in blood of HIV+ women was mirrored in the cervical mucosa and HPV co-infection was linked to lower levels of mucosal CD4 T cells in HIV+ women (%median: 22 vs 32; p = 0.04). In addition, HIV and HPV infection, and especially HPV-associated cervical lesions were linked to significantly higher frequencies of HLA-DR+ CD4 and CD8 T cells (p-values < 0.05). Interestingly, HPV infection did not significantly alter frequencies of CCR5+ or α4β7+ CD4 T cells.ConclusionThe increased proportion of activated cervical T cells associated with HPV and HIV infection, as well as HPV-associated lesions, together with the HIV-induced depletion of cervical CD4 T cells, may increase the risk for HPV infection, associated premalignant lesions and cancer in HIV+ women. Further, high levels of activated CD4 T cells associated with HPV and HPV-associated lesions could contribute to a higher susceptibility to HIV in HPV infected women.

Highlights

  • Human Immunodeficiency Virus (HIV) and Human Papilloma Viruses (HPV) are both sexually transmitted viruses that cause chronic infections and disease [1,2]

  • The skewed CD4/CD8 T cell ratio in blood of HIV+ women was mirrored in the cervical mucosa and HPV co-infection was linked to lower levels of mucosal CD4 T cells in HIV+ women (% median: 22 vs 32; p = 0.04)

  • HIV and HPV infection, and especially HPV-associated cervical lesions were linked to significantly higher frequencies of Human Leukocyte Antigen–DR isotype (HLA-DR)+ CD4 and CD8 T cells (p-values < 0.05)

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Summary

Introduction

Human Immunodeficiency Virus (HIV) and Human Papilloma Viruses (HPV) are both sexually transmitted viruses that cause chronic infections and disease [1,2]. HPVs are a family of about 200 types of small, non-enveloped double-stranded DNA viruses which infect epithelial cells [3]. Depending on their oncogenic propensity, HPV group into either low-risk HPV (LR-HPV) or high-risk HPV (HR-HPV).HR-HPV types HPV16 and HPV18 together are linked to over 70% of all cervical cancer (CC) cases worldwide [4]. In contrast to most AIDS-defining diseases, the burden of HPV-associated premalignant and malignant lesions remains high in HIV infected individuals despite the initiation of ART [7]. The burden of HPV-associated premalignant and malignant cervical lesions remains high in HIV+ women even under ART treatment. In order to identify possible underlying pathophysiologic mechanisms, we studied activation and HIV co-receptor expression in cervical T-cell populations in relation to HIV, HPV and cervical lesion status

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