# Somatic hypermutation and rescue from self-reactivity in Pre-B lymphocytes

> **NIH NIH R21** · EMORY UNIVERSITY · 2020 · $257,320

## Abstract

PROJECT SUMMARY
The generation of B cell receptor diversity is mediated by RAG recombinases, and it occurs during
B cell development in the bone marrow. This is brought about by stochastic rearrangement of
V(D)J gene segments to assemble the B cell receptor. These stochastic rearrangements also
lead to the development of B cells that recognize self-antigens. These self-reactive B cell clones
are dealt with by either clonal deletion, clonal anergy or RAG recombinase-mediated rescue of
self-reactive clones by V gene segment replacement. In this proposal, we present an additional
mechanism by which autoreactive pre-B cells are rescued from self-reactivity. We propose that
Activation-induced Cytidine Deaminase (AID) plays a role in rescuing self-reactive pre-B cells.
AID induces two significant genetic alterations in antigen-activated mature B cells; somatic
hypermutation and class switch recombination. The former generates high-affinity B cell mutants
that are enticed to enter the memory pool, and the latter facilitates Ig isotype switching from IgM
to IgG, IgA or IgE.
Interestingly, it has been known for over two decades that a small fraction of immature, bone
marrow pre-B cells undergo class switching. This is perplexing because it occurs even in pre-B
cells which have only rearranged their Ig heavy chain and are yet to rearrange their light chains.
We, based on very preliminary data may have an answer to this puzzle. Our central hypothesis
is that immature, self-reactive pre-B cells turn on AID and undergo somatic mutation in order to
alter their specificity from self- to non-self-reactivity. The class switching that occurs in these bone
marrow pre-B cells is a collateral consequence of AID expression. We will test our central
hypothesis in two aims. The proposed work is significant because, upon completion, we will have
established a new paradigm to explain the rescue of pre-B cells from self-reactivity. We are well-
positioned to carry out the proposed studies as our team with the addition of collaborator Dr.
Ignacio Sanz, one of the world’s premier experts on autoimmunity, has the requisite collective
expertise to complete the proposed studies successfully.

## Key facts

- **NIH application ID:** 9877319
- **Project number:** 1R21AI149252-01
- **Recipient organization:** EMORY UNIVERSITY
- **Principal Investigator:** JOSHY JACOB
- **Activity code:** R21 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2020
- **Award amount:** $257,320
- **Award type:** 1
- **Project period:** 2020-05-01 → 2022-04-30

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/9877319

## Citation

> US National Institutes of Health, RePORTER application 9877319, Somatic hypermutation and rescue from self-reactivity in Pre-B lymphocytes (1R21AI149252-01). Retrieved via AI Analytics 2026-05-23 from https://api.ai-analytics.org/grant/nih/9877319. Licensed CC0.

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