Please ensure Javascript is enabled for purposes of website accessibility
Home > Support > Flow Lab Notes & OMIP Reviews

Panel for Flow Cytometry Detection of Helper T Cells

Release date: 2025-10-30 View count: 23

What are Helper T Cells?

Helper T cells (Th cells) are one of the most important lymphocyte subpopulations in the immune system, primarily composed of CD4+ T cells. They play a crucial role in immune responses by acting as "commanders," coordinating the body's defence and immune homeostasis. This is achieved through the secretion of cytokines, aiding B cells in antibody production, enhancing macrophage-mediated pathogen clearance, and regulating the functions of other immune cells. Dysfunctions in Helper T cells are often linked to immune-related diseases such as infection intolerance, allergic reactions, autoimmune diseases, or tumour immune escape.

Figure 1. Helper T Cells and Immune Responses in Different Tissues (DOI: 10.1093/intimm/dxw006)

Differentiation of Helper T Cells

Naive CD4+ T cells are activated via their T cell receptor (TCR) in conjunction with co-stimulatory molecules like CD28, and through antigen-presenting cells (APCs) that express major histocompatibility complex (MHC) class II molecules, such as macrophages, dendritic cells, and B cells. Activation signals are transmitted through the recognition and binding of MHC II molecules presenting homologous antigen peptides on the surface. Upon complete activation, naive CD4+ T cells rapidly proliferate and differentiate into various subsets of Helper T cells, such as Th1, Th2 or Th17 (Figure 2).

Figure 2. Development of CD4+ T Cells and Their Functional Subsets in Immunity (DOI: 10.3389/fimmu.2021.669474)

Helper T Cells and Disease

The balance of Helper T cell subsets is crucial for immune homeostasis, and imbalance often leads to disease development. For instance, an imbalance between Th1/Th2 cells is associated with susceptibility to allergies or infections, while excessive activation of Th17 cells is linked to autoimmune diseases such as rheumatoid arthritis and psoriasis. Defects in Treg function may result in graft rejection and failure of immune tolerance. In tumour immunotherapy, different Helper T cell subsets can provide important prognostic and therapeutic insights. Therefore, accurate and systematic detection of Helper T cell subsets is vital for both research and clinical applications.

Figure 3. Th Cells and Type II Immune Responses (DOI: 10.1038/nri.2017.118)

Flow Cytometric Detection of Helper T Cells

Flow cytometry is a critical method for detecting Helper T cells and their subsets in both research and clinical settings. By analysing surface markers, secreted cytokines, and transcription factors, it allows for efficient identification and quantification of different subsets.

Table 1. Helper T Cell Subsets and Markers

Cell Subset

Surface Markers

Secreted Cytokines

Transcription Factors

Th1

CD4, CD183(CXCR3)*, CD195(CCR5), CD197(CCR7), CXCL9, CXCL10, CXCL11

IFN-γ*, LT-α, TNF, Perforin, Granzyme A, Granzyme B, Granulysin (Hu)

T-bet*, STAT1, STAT4, Runx3

Th2

CD4, CD194(CCR4), CD294(CRTH2)*, CD193(CCR3), CD198(CCR8), MDC, TCA3, TARC

IL-4*, IL-5,  IL-6, IL-10, IL-13, IL-31

GATA3*, STAT5, STAT6, MAF, GFI-1, IRF4, c-Maf

Th9

CD4, CCL20, CD196(CCR6)

IL-9*, IL-10, CCL17 (TARC), CCL22 (MDC),TGF-β

GATA3 (early), SMADs, STAT6, PU.1,  IRF4

Th17

CD4, CD161, CD194(CCR4), CD196(CCR6)*, IL23R, CCL4, CCL17, CCL22

IL-17A*, IL-17F, IL-21, IL-22, IL-24, IL-26 (Hu), TNF, CCL20 (MIP-3α)

RORγt*, RORα4, STAT3, Runx1, Batf, IRF4, c-Maf

Th22

CD4, CCR10, CD194(CCR4), CD196(CCR6), CD279 (PD-1)

IL-22*, TNF

AhR*

Tfh

CD4, CD185 (CXCR5)*, CD196(CCR6), CD278 (ICOS)*, CD279 (PD-1)*

IFN-γ, IL-4, IL-17A, IL-17F, IL-21*

Bcl-6* , MAF,  STAT3

Treg

CD4, CD25*, CD127*-/low, CD152(CTLA4)

IL-10, IL-35, TGF-β

Foxp3*, Smad3, STAT5, AhR

*Note: * indicates characteristic markers of cells.

abinScience Recommended Flow Cytometry Antibodies for Helper T Cell Detection

Target

Clone

Species

Localization

CD3

OKT3

Human

Surface

CD4

SAA0002

Human

Surface

CD8

G10-1

Human

Surface

CD25

1H4

Human

Surface

CD127

N13B2-h3

Human

Surface

CD183

V3G6

Human

Surface (Chemokine receptor)

CD185

16D7

Human

Surface (Chemokine receptor)

CD193

5E8-G9-B4

Human

Surface (Chemokine receptor)

CD194

SAA0069

Human

Surface (Chemokine receptor)

CD195

PRO-140

Human

Surface (Chemokine receptor)

CD196

R612

Human

Surface (Chemokine receptor)

CD197

R707

Human

Surface (Chemokine receptor)

CD198

SAA1405

Human

Surface (Chemokine receptor)

CXCL9

SAA0465

Human

Secreted (Chemokines)

CXCL10

SAA0413

Human

Secreted (Chemokines)

CXCL11

SAA0466

Human

Secreted (Chemokines)

TCA3CCL1

SAA0526

Human

Secreted (Chemokines)

TARCCCL17

SAA0460

Human

Secreted (Chemokines)

IFNγ

SAA0414

Human

Secreted (Cytokines)

IL4

SAA0371

Human

Secreted (Cytokines)

IL9

SAA0377

Human

Secreted (Cytokines)

IL17A

SAA0386

Human

Secreted (Cytokines)

IL22

SAA0391

Human

Secreted (Cytokines)

GATA3

SAA0103

Human

Transcription Factor

FOXP3

1A210

Human

Transcription Factor

CD3

145-2C11

Mouse

Surface

CD4

GK1.5

Mouse

Surface

CD8

53-6.72

Mouse

Surface

CD25

PC61/PC61.5.3

Mouse

Surface

IFNγ

XMG1.2

Mouse

Secreted (Cytokines)

IL4

11B11

Mouse

Secreted (Cytokines)

IL17A

BZN035

Mouse

Secreted (Cytokines)

About Us

abinScience was founded in France and is focused on the development and production of high-quality life science reagents. Based in the innovative technology hub of Strasbourg, France, our vision is to "Empower Bioscience Discovery." Our flow cytometry antibody products cover common detection markers and are available in a wide range, catering to multi-species research needs. We offer stable and reliable support for scientific research. For more information on our flow cytometry antibodies, please visit: www.abinscience.com

References   

[1] Basu A, Ramamoorthi G, Albert G, Gallen C, Beyer A, Snyder C, Koski G, Disis ML, Czerniecki BJ, Kodumudi K. Differentiation and Regulation of TH Cells: A Balancing Act for Cancer Immunotherapy. Front Immunol. 2021 May 3;12:669474.

[2] Walker JA, McKenzie ANJ. TH2 cell development and function. Nat Rev Immunol. 2018 Feb;18(2):121-133.

[3] Luckheeram RV, Zhou R, Verma AD, Xia B. CD4⁺T cells: differentiation and functions. Clin Dev Immunol. 2012;2012:925135.

[4] Nakayama T, Hirahara K, Onodera A, Endo Y, Hosokawa H, Shinoda K, Tumes DJ, Okamoto Y. Th2 Cells in Health and Disease. Annu Rev Immunol. 2017 Apr 26;35:53-84.

[5] Mills KHG. IL-17 and IL-17-producing cells in protection versus pathology. Nat Rev Immunol. 2023 Jan;23(1):38-54.

[6] Geng J, Yu S, Zhao H, Sun X, Li X, Wang P, Xiong X, Hong L, Xie C, Gao J, Shi Y, Peng J, Johnson RL, Xiao N, Lu L, Han J, Zhou D, Chen L. The transcriptional coactivator TAZ regulates reciprocal differentiation of TH17 cells and Treg cells. Nat Immunol. 2017 Jul;18(7):800-812.

Get a free quote