# Innate Immune Surveillance of HIV-1 During Transmission and Systemic Infection

> **NIH NIH R01** · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · 2021 · $563,051

## Abstract

Project Summary
Innate immune responses represent one of the first and most potent lines of defense against infection.
Importance of this surveillance network is underscored by the numerous mechanisms that pathogens have
evolved to counteract and evade these responses. The success of the immediate innate immune response
relies on the recognition of conserved structures, termed pathogen associated molecular patterns (PAMPs),
commonly present in microbes but not in the host. Pattern recognition receptors (PRRs) act as microbial
sensors for the host. The sensing of PAMPs by host PRRs initiate the induction of several intracellular
signaling events, triggering the expression of cytokines and interferons, which can govern potent restrictors of
pathogen infection. In this application, we propose to pursue the hypothesis that a robust innate immune
recognition and response to HIV-1 exposure, likely elicited from abortive infection of myeloid cells, rises from
the activation of key pattern recognition receptor (PRR) pathways and results in a localized antiviral
environment that markedly decreases the likelihood of CD4+ T cell infection and subsequent spread of
infection, both in the mucosa and during peripheral infection. The cGAS cytoplasmic DNA sensing pathway,
which is particularly active in myeloid cells, has recently been identified as a key sensor for reverse transcribed
HIV-1 DNA. Activation of this and potentially other PRR-governed pathways promote the secretion of
interferons (IFNs) leading to the transcription of hundreds of interferon-stimulated genes (ISGs), some of which
contribute to suppression of HIV-1 replication. Recently, we have reported the identification PQBP1 as a critical
component in the recognition of early HIV-1 nucleic acid products required for activation of the cGAS DNA
sensing pathway, resulting IFN induction in HIV-infected myeloid cells. Here, we propose to investigate in more
detail the regulation of this novel sensing circuit, including understanding the features and accessibility of the
HIV-1 PAMP, its downstream regulation, and its impact in HIV-1 transmission. A better understanding of the
innate response circuitry that senses HIV-1 infection is likely to enable the development of novel therapeutic
interventions against systemic HIV-1 infection, and the illumination of the molecular basis of a protective
mucosal innate response to HIV-1 will be critical in next generation vaccine and adjuvant design.

## Key facts

- **NIH application ID:** 10086947
- **Project number:** 5R01AI127302-05
- **Recipient organization:** SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE
- **Principal Investigator:** SUMIT K CHANDA
- **Activity code:** R01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2021
- **Award amount:** $563,051
- **Award type:** 5
- **Project period:** 2017-02-28 → 2022-03-02

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10086947

## Citation

> US National Institutes of Health, RePORTER application 10086947, Innate Immune Surveillance of HIV-1 During Transmission and Systemic Infection (5R01AI127302-05). Retrieved via AI Analytics 2026-05-23 from https://api.ai-analytics.org/grant/nih/10086947. Licensed CC0.

---

*[NIH grants dataset](/datasets/nih-grants) · CC0 1.0*