Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6063491 | Journal of Allergy and Clinical Immunology | 2015 | 15 Pages |
Abstract
Specific mutations affect the quantity and quality of cTFH cells, highlighting the need to assess TFH cells in patients by using multiple criteria, including phenotype and function. Furthermore, IFN-γ functions in vivo to restrain TFH cell-induced B-cell differentiation. These findings shed new light on TFH cell biology and the integrated signaling pathways required for their generation, maintenance, and effector function and explain the compromised humoral immunity seen in patients with some PIDs.
Keywords
Bcl-6T-dependentIL-21 receptorIL-21RIL-10 receptorIL-10RcTfhB-cell lymphoma 6IL-12RPD-1follicular helper TTFHTFRGOFTregLOFPIDSTATprimary immunodeficienciesloss of functionHumoral immunityGain of functiondouble-positivedouble-negativeFollicular helper T cellscytokine signalingSignal transducer and activator of transcriptionGerminal centerProgrammed death 1Regulatory T primary immunodeficiencyIL-12 receptor
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Authors
Cindy S. PhD, Natalie BSc Hons, Geetha MSc, Danielle T. BApplSci, James MPhil, Thomas BSc Hons, Jacinta MD, PhD, Satoshi MD, PhD, Jennifer L. BS, Elissa K. PhD, Simon J. MSc, Kathryn BSc Hons, Stéphanie PhD, Anne PhD, Masao MD, PhD, Peter D. FRCPCH,