Molecular Signatures of Immune Activation and Epithelial Barrier Remodeling Are Enhanced during the Luteal Phase of the Menstrual Cycle: Implications for HIV Susceptibility

被引:44
|
作者
Birse, Kenzie [1 ,2 ]
Arnold, Kelly B. [3 ,4 ]
Novak, Richard M. [6 ]
McCorrister, Stuart [5 ]
Shaw, Souradet [9 ]
Westmacott, Garrett R. [5 ]
Ball, Terry B. [1 ,2 ,7 ]
Lauffenburger, Douglas A. [3 ,4 ]
Burgener, Adam [1 ,2 ,8 ]
机构
[1] Publ Hlth Agcy Canada, Natl Lab HIV Immunol, JC Wilt Infect Dis Res Ctr, Winnipeg, MB, Canada
[2] Univ Manitoba, Dept Med Microbiol, Winnipeg, MB, Canada
[3] MIT, Dept Biol Engn, Cambridge, MA 02139 USA
[4] MIT, Ctr Gynepathol Res, Cambridge, MA 02139 USA
[5] Natl Microbiol Lab, Mass Spectrometry Core Facil, Winnipeg, MB, Canada
[6] Univ Illinois, Dept Med, Chicago, IL USA
[7] Univ Nairobi, Dept Med Microbiol, Nairobi, Kenya
[8] Karolinska Inst, Karolinska Univ Hosp, Infect Dis Unit, Dept Med Solna,Ctr Mol Med, Stockholm, Sweden
[9] Univ Manitoba, Dept Community Hlth Sci, Winnipeg, MB R3T 2N2, Canada
基金
加拿大健康研究院;
关键词
FEMALE GENITAL-TRACT; HORMONAL CONTRACEPTIVES; CYSTATIN ANTIPROTEASES; INNATE IMMUNITY; T-CELLS; WOMEN; PROTECTION; IDENTIFICATION; PROTEINS; SERPIN;
D O I
10.1128/JVI.00756-15
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The variable infectivity and transmissibility of HIV/SHIV has been recently associated with the menstrual cycle, with particular susceptibility observed during the luteal phase in nonhuman primate models and ex vivo human explant cultures, but the mechanism is poorly understood. Here, we performed an unbiased, mass spectrometry-based proteomic analysis to better understand the mucosal immunological processes underpinning this observed susceptibility to HIV infection. Cervicovaginal lavage samples (n = 19) were collected, characterized as follicular or luteal phase using days since last menstrual period, and analyzed by tandem mass spectrometry. Biological insights from these data were gained using a spectrum of computational methods, including hierarchical clustering, pathway analysis, gene set enrichment analysis, and partial least-squares discriminant analysis with LASSO feature selection. Of the 384 proteins identified, 43 were differentially abundant between phases (P < 0.05, >= 2-fold change). Cell-cell adhesion proteins and anti-proteases were reduced, and leukocyte recruitment (interleukin-8 pathway, P = 1.41E-5) and extravasation proteins (P = 5.62E-4) were elevated during the luteal phase. LASSO/PLSDA identified a minimal profile of 18 proteins that best distinguished the luteal phase. This profile included cytoskeletal elements and proteases known to be involved in cellular movement. Gene set enrichment analysis associated CD4(+) T cell and neutrophil gene set signatures with the luteal phase (P< 0.05). Taken together, our findings indicate a strong association between proteins involved in tissue remodeling and leukocyte infiltration with the luteal phase, which may represent potential hormone-associated mechanisms of increased susceptibility to HIV. IMPORTANCE Recent studies have discovered an enhanced susceptibility to HIV infection during the progesterone-dominant luteal phase of the menstrual cycle. However, the mechanism responsible for this enhanced susceptibility has not yet been determined. Understanding the source of this vulnerability will be important for designing efficacious HIV prevention technologies for women. Furthermore, these findings may also be extrapolated to better understand the impact of exogenous hormone application, such as the use of hormonal contraceptives, on HIV acquisition risk. Hormonal contraceptives are the most widely used contraceptive method in sub-Saharan Africa, the most HIV-burdened area of the world. For this reason, research conducted to better understand how hormones impact host immunity and susceptibility factors important for HIV infection is a global health priority.
引用
收藏
页码:8793 / 8805
页数:13
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