# Protective humoral immunity to influenza infection

> **NIH NIH R01** · UNIVERSITY OF CALIFORNIA AT DAVIS · 2020 · $485,276

## Abstract

PROJECT SUMMARY
The extrafollicular (EF) B cell response generates virus-specific IgM, IgG and IgA in the airway lumen
and local lymph nodes as early as 72h after influenza virus infection, correlating temporally with virus
clearance. EF responses are distinct in kinetics, function and signaling requirements from the slower
germinal center responses. EF B cell responses habe been largely dismissed as significant in pathogen-
induced immunity, as they are though to generate only short-lived plasma cells and low affinity antibodies.
Yet, consistent with recent studies on a requirement for high-affinity interaction between BCR and
antigen for induction of EF responses, our studies show that a prototypic EF response to HA of influenza
A/Puerto Rico /8/34 generates high-affinity protective antibodies long-term after influenza infection. Thus,
identifying this response as a crucial component of primary influenza-infection-induced antiviral immunity.
However, immunization with inactivated virus in adjuvant failed to induce EF responses, yet did induce
strong germinal centers, thereby identifying a specific deficit in vaccine-induced humoral immunity, that
may reduce its efficacy. Because the signals inducing EF responses are unknown, and their protective
capacity is unclear, they cannot be exploited for therapeutic or prophylactic uses. To overcome this
knowledge gap we propose to test our hypothesis that innate B cell direct signaling drives high affinity
long-term protective antiviral humoral immunity via induction of strong EF responses. Specific Aim #1 will
use gene-targeted mice to identify the receptors and signaling pathways responsible for EF development
after influenza infection and complement inactivated influenza vaccines with their corresponding ligands
to generate EF responses. Aim 2 will delineate the molecular targets of these signaling pathways for the
differentiation of B cells to EF plasma blasts, following the fate of influenza HA-specific B cells. Aim 3 will
assess the quality and protective capacity of EF and GC B cell responses. Successful outcome of these
studies will provide a conceptual advance by demonstrating that EF responses to infection can generate
high-affinity antibody responses and provide immune protection. Identification of the ligands, signaling
pathways and the gene targets that drive EF responses will increase fundamental knowledge on the
mechanisms of B cell differentiation and open the door for the exploitation of EF responses to enhance
immunity through therapeutic and prophylactic interventions.

## Key facts

- **NIH application ID:** 9948551
- **Project number:** 5R01AI117890-05
- **Recipient organization:** UNIVERSITY OF CALIFORNIA AT DAVIS
- **Principal Investigator:** Nicole Baumgarth
- **Activity code:** R01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2020
- **Award amount:** $485,276
- **Award type:** 5
- **Project period:** 2016-06-09 → 2023-05-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/9948551

## Citation

> US National Institutes of Health, RePORTER application 9948551, Protective humoral immunity to influenza infection (5R01AI117890-05). Retrieved via AI Analytics 2026-05-26 from https://api.ai-analytics.org/grant/nih/9948551. Licensed CC0.

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