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University of Minnesota

The Function of PTPN22 and the Autoimmune Risk Variant LypW in Immune Responses to Vaccination

Abstract

dc:description.abstract

High-affinity antibody production, T cell activation, and Interferon upregulation all contribute to protective immunity that occurs in humans following influenza immunization. Hematopoietic cell-specific PTPN22 encodes Lymphoid Phosphatase (Lyp), which regulates lymphocyte antigen receptor and Pattern Recognition Receptor (PRR) signaling. A PTPN22 variant R620W (LypW) predisposes to autoimmune and infectious disease, and confers altered signaling through antigen receptors and PRRs. We tested the hypothesis that LypW-bearing humans would have diminished immune response to trivalent influenza vaccine (TIV). LypW carriers exhibited decreased induction of influenza-specific CD4 T cells expressing effector cytokines, and failed to increase antibody affinity following TIV. No differences between LypW carriers and non-carriers were observed in virus-specific CD8 T cell responses, early interferon transcriptional responses, or myeloid APC costimulatory molecule upregulation. LypW association with defects in TIV-induced CD4 T cell expansion and antibody affinity maturation suggests that LypW may predispose to diminished capacity to generate protective immunity against influenza.

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Crabtree, Juliet

Subjects

dc:subject × 2

Rights

Language dc:language.iso
en

Identifiers

dc:identifier.*
Handle dc:identifier.uri
http://hdl.handle.net/11299/182251
OAI identifier oai:identifier
oai:conservancy.umn.edu:11299/182251

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University of Minnesota
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Last updated
2026-07-24
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citation

Crabtree, Juliet. The Function of PTPN22 and the Autoimmune Risk Variant LypW in Immune Responses to Vaccination. 2016. http://hdl.handle.net/11299/182251