Although anal intercourse is a common mode of HIV-1 transmission, particularly for men who have sex with men, many fundamental and mechanistic questions remain. The long-term objective of this study is to understand the early events in HIV-1 rectal transmission and to gain new insights, which will potentially lead to new intervention strategies, including vaccines and topical microbicides optimized for rectal use. Studying HIV-1 vaginal transmission in the highly relevant SIV-rhesus macaque model has revealed important events critical for transmission, such as target cell availability, innate immune response, and inflammation at the portal of entry, all factors which play a key role in transmission. Because the anatomical/histological features and the physiological functions of vagina and cervix differ from the rectum, we hypothesize that the underlying mechanisms and timing of HIV-1 rectal transmission will significantly differ from those of vaginal-cervical transmission. Utilizing innovative approaches and an established conceptual framework from studies of vaginal transmission, we will test this hypothesis by investigating three specific aims: 1) determine the timing, location, spatial distribution and cell types of virus-infected cells at the portal of entry and in draining and distal lymphatic tissues;2) determine relationships between virus and susceptible target cells (CD4+ T cells, macrophages, and dendritic cells) and between virus-infected cells and the mucosal innate immune response in the rectum shortly after intra-rectal SIV inoculation, thereby determining whether changes in target-cell availability play a critical role in local expansion and systemic spread of infection;and 3) determine the spatial relationships and ratio of virus-specific CD8+ T effector cells (E) and virus-infected-target cells (T) at the portal of entry and in other tissue compartments to extent of control of virus replication, using a novel procedure combining in-situ tetramers and in-situ hybridization The proposed research is significant as it is expected to reveal important mechanisms underlying rectal transmission and potentially provide guidance for designing anti-HIV-1 vaccines and topical microbicides.

Public Health Relevance

The proposed studies are relevant to public health because unprotected anal intercourse is a common mode for HIV-1 transmission, especially in men who have sex with men. Thus, by studying for HIV-1 rectal transmission, new knowledge will be gained to aid HIV-1 vaccine and microbicide design and development.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
7R01DK087625-02
Application #
8119932
Study Section
AIDS Immunology and Pathogenesis Study Section (AIP)
Program Officer
Hamilton, Frank A
Project Start
2010-08-15
Project End
2014-07-31
Budget Start
2010-08-15
Budget End
2011-07-31
Support Year
2
Fiscal Year
2010
Total Cost
$371,430
Indirect Cost
Name
University of Nebraska Lincoln
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
555456995
City
Lincoln
State
NE
Country
United States
Zip Code
68588
Fan, Wenjin; Demers, Andrew James; Wan, Yanmin et al. (2018) Altered Ratio of T Follicular Helper Cells to T Follicular Regulatory Cells Correlates with Autoreactive Antibody Response in Simian Immunodeficiency Virus-Infected Rhesus Macaques. J Immunol 200:3180-3187
Yuan, Zhe; Ma, Fangrui; Demers, Andrew J et al. (2017) Characterization of founder viruses in very early SIV rectal transmission. Virology 502:97-105
Vargas-Inchaustegui, Diego A; Demers, Andrew; Shaw, Julia M et al. (2016) Vaccine Induction of Lymph Node-Resident Simian Immunodeficiency Virus Env-Specific T Follicular Helper Cells in Rhesus Macaques. J Immunol 196:1700-10
Lu, Wuxun; Demers, Andrew J; Ma, Fangrui et al. (2016) Next-Generation mRNA Sequencing Reveals Pyroptosis-Induced CD4+ T Cell Death in Early Simian Immunodeficiency Virus-Infected Lymphoid Tissues. J Virol 90:1080-7
Yuan, Zhe; Kang, Guobin; Ma, Fangrui et al. (2016) Recapitulating Cross-Species Transmission of Simian Immunodeficiency Virus SIVcpz to Humans by Using Humanized BLT Mice. J Virol 90:7728-39
Li, Yue; Kang, Guobin; Duan, Lijie et al. (2015) SIV Infection of Lung Macrophages. PLoS One 10:e0125500
Li, Qingsheng; Tso, For Yue; Kang, Guobin et al. (2015) Early Initiation of Antiretroviral Therapy Can Functionally Control Productive HIV-1 Infection in Humanized-BLT Mice. J Acquir Immune Defic Syndr 69:519-27
Barrenas, Fredrik; Palermo, Robert E; Agricola, Brian et al. (2014) Deep transcriptional sequencing of mucosal challenge compartment from rhesus macaques acutely infected with simian immunodeficiency virus implicates loss of cell adhesion preceding immune activation. J Virol 88:7962-72
Lu, Wuxun; Ma, Fangrui; Churbanov, Alexander et al. (2014) Virus-host mucosal interactions during early SIV rectal transmission. Virology 464-465:406-414
Demers, Andrew; Kang, Guobin; Ma, Fungrui et al. (2014) The mucosal expression pattern of interferon-? in rhesus macaques. J Leukoc Biol 96:1101-7