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Methods for Studying T Helper Cells in Humans and Mice
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Guest Editor

Qin Xu

Qin Xu

Laboratory of Pamela Schwartzberg, Cell Signaling and Immunity Section, Laboratory of Immune System Biology, NIAID, NIH, Bethesda, MD, United States

Dr. Xu obtained her M.D. in Clinical Medicine from Zhejiang University (2009) and worked in pediatrics at the Children's Hospital affiliated with Zhejiang University until 2014. She earned her Ph.D. in Immunology from Zhejiang University in 2019, focusing on key regulatory genes in T helper cell differentiation by utilizing conditional gene knockout mice. She continued her work by conducting assessments on patients with autoimmune diseases after joining as a rheumatologist at Sir Run Run Shaw Hospital in 2019. Currently, she is a postdoctoral visiting fellow at NIAID (NIH), primarily engaged research on adaptive immune responses in pharyngeal tissues following SARS-CoV-2 infection and/or vaccination in Dr. Pamela Schwartzberg's lab.

Collection Overview

T helper cells play a central role in orchestrating adaptive immune responses. Extensive research has identified five primary CD4 T helper cell (Th) subsets: Th1, Th2, Th17, Treg (T regulatory), and Tfh (follicular T helper) cells. Additionally, less common T helper subsets, including "Th3", "Th9", and "Th22" cells, as well as subsets of Tregs, have also been recognized. Their roles in various diseases and immune responses make them a critical focus of research in immunology and medicine. This Methods Collection will spotlight both established and emerging techniques related to T helper cell research. It will offer cutting-edge and reproducible protocols with a focus on: 

  1. Studying the in vivo and in vitro development of T helper cells 
  2. Investigating tissue-resident T helper cells 
  3. Utilizing the CRISPR-Cas9 screening system in T helper cell research 
  4. Exploring methods for studying human T helper cells

Articles

Retroviral CRISPR/Cas9-Mediated Gene Targeting for the Study of Th17 Differentiation in Vitro
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Retroviral CRISPR/Cas9-Mediated Gene Targeting for the Study of Th17 Differentiation in Vitro

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2024

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