Grants > Investigating Autoimmune Contributions to Alzheimer’s Disease Updated On: Jul 2, 2026
Alzheimer's Disease Research Grant

Investigating Autoimmune Contributions to Alzheimer’s Disease

Immunity & Inflammation
Jennifer Yokoyama, PhD.

Principal Investigator

Jennifer Yokoyama, PhD

University of California, San Francisco

San Francisco, CA, United States

About the Research Project

Program

Alzheimer's Disease Research

Award Type

Standard

Award Amount

$299,548

Active Dates

July 01, 2026 - June 30, 2029

Grant ID

A2026031S

Co-Principal Investigator(s)

Joseph Sabatino, MD, PhD, University of California, San Francisco

Goals

Our study will analyze blood and spinal fluid samples across the clinical spectrum of Alzheimer’s disease (AD) to determine whether (i) a subset of AD patients possess autoantibodies (which recognize self-proteins) and (ii) female sex associates with an inflammatory transcript and protein profile.

Summary

Given that genetic and clinical evidence suggests a link between autoimmune disease and Alzheimer’s disease (AD) risk, our study will use advanced sequencing technologies to determine whether AD patients possess self-targeted autoantibodies in their blood or brain that may drive disease. Additionally, we will explore whether female sex is associated with an increase of pro-inflammatory proteins or transcripts. Our study has the potential to identify a subset of AD patients who possess an immune-mediated form of disease and that may benefit from the development of targeted immunotherapies.

Unique and Innovative

Our study will represent the first large-scale, comprehensive survey of autoantibody signatures across the clinical spectrum of AD. We will also examine inflammatory associations with female sex, an understudied aspect of AD biology.

Foreseeable Benefits

Ultimately, our study could identify whether a subset of AD patients possess autoantibody or hyper-inflammatory signatures in their blood or spinal fluid. By successfully identifying this subset of patients, our study would enrich our understanding of AD pathogenesis and clinical heterogeneity. Furthermore, this study could reveal new avenues for immunotherapeutic intervention, such as candidate pathways and targets for future drug discovery initiatives.