Jason S. Stumhofer
Associate Professor
University of Arkansas for Medical Sciences
faculty
Microbiology & Immunology, College of Medicine
Research Areas
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Biography and Research Information
OverviewAI-generated summary
Jason S. Stumhofer's research program investigates the adaptive immune system, with a particular focus on B cell and T cell responses during parasitic and viral infections. His group studies the cellular and molecular mechanisms that regulate the formation and function of germinal centers, key sites for antibody production and affinity maturation.
Stumhofer has received federal funding from the NIH/National Institute of Allergy and Infectious Diseases for two projects. The first, totaling $76,000, focuses on the design of a B cell tetramer to track specific B cells responding to Plasmodium falciparum merozoite surface protein 2 (PfMSP2). The second grant, for $185,375, investigates the regulation of macrophage function during acute Plasmodium infection.
His publications include studies on the heterogeneity of memory B cell populations, the role of ICOS in germinal center maintenance, and the intrinsic p53 activation's restriction of gammaherpesvirus-driven B cell expansion. Stumhofer has an h-index of 26 with over 5,200 citations across his 52 publications. He collaborates with researchers at the University of Arkansas for Medical Sciences, including Enatha Ntirandekura, Kara A. O’Neal, Camille L. Foscue, and Susie L. Brown.
Metrics
- h-index: 26
- Publications: 52
- Citations: 5,276
Selected Publications
- Intrinsic p53 activation restricts gammaherpesvirus driven germinal center B cell expansion during latency establishment (2025) DOI
- Bhlhe40 limits early IL-10 production from CD4 <sup>+</sup> T cells during <i>Plasmodium yoelii</i> 17X infection (2023) DOI
- IgM+ and IgM– memory B cells represent heterogeneous populations capable of producing class-switched antibodies and germinal center B cells upon rechallenge with <i>P. yoelii</i> (2022) DOI
- Towards rainbow portable Cytophone with laser diodes for global disease diagnostics (2022) DOI
- ICOS Expression Is Required for Maintenance but Not the Formation of Germinal Centers in the Spleen in Response to Plasmodium yoelii Infection (2022) DOI
- ICOS expression is required for maintenance but not the formation of germinal centers in the spleen in response to <i>P. yoelii</i> infection (2021) DOI
- IgM <sup>+</sup> and IgM <sup>-</sup> memory B cells represent heterogeneous populations capable of producing class-switched antibodies and germinal center B cells upon re-challenge with <i>P. yoelii</i> (2021) DOI
Federal Grants 2 $261,375 total
Regulation of macrophage function during acute infection with Plasmodium
Design of a B cell tetramer to track PfMSP2-specific B cells
Grants & Funding
- Regulation of macrophage function during acute infection with Plasmodium NIH/Nat. Inst. of Allergy & Infectious Diseases Principal Investigator
- Stumhofer Start up Account UAMS College of Medicine Principal Investigator
- A protective role for IL-17 in blood-stage malaria NIH Principal Investigator
- No FP attached UAMS College of Medicine Principal Investigator
- Multicolor Photoacoustic Malaria Detector NIH Co-Investigator
- Understanding the contribution of atypical B cell progenitors to the humoral response NIH Principal Investigator
- Design of a B cell tetramer to track PfMSP2-specific B cells NIH/Nat. Inst. of Allergy & Infectious Diseases Principal Investigator
- Regulation and function of B cells during malaria infection- Resubmission NIH Principal Investigator
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