Related Experiment Video
Updated: Aug 23, 2025

A Protocol for the Production of KLRG1 Tetramer
Published on: January 12, 2010
KLMab-1: An Anti-human KLRG1 Monoclonal Antibody for Immunocytochemistry
Masaki Saito1, Hiroyuki Suzuki1, Teizo Asano2
1Department of Molecular Pharmacology, Tohoku University Graduate School of Medicine, Sendai, Miyagi, Japan.
Insights
Researchers developed a new antibody targeting Killer cell lectin-like receptor subfamily G member 1 (KLRG1), a key molecule in immune responses. This antibody is effective for detecting KLRG1 in both laboratory settings and human immune cells, aiding cancer immunotherapy research.
Area of Science:
- Immunology
- Cancer Research
- Monoclonal Antibody Development
Background:
- Immune checkpoint molecules are crucial targets for cancer immunotherapy.
- Killer cell lectin-like receptor subfamily G member 1 (KLRG1) is an immune checkpoint molecule found on T and NK cells.
- KLRG1 plays a role in antiviral and antitumor immunity, with upregulated expression in certain diseases and tumors.
Purpose of the Study:
- To develop and validate monoclonal antibodies (mAbs) against human KLRG1 (hKLRG1) for diagnostic and therapeutic applications.
- To assess the utility of anti-hKLRG1 mAbs in detecting both exogenous and endogenous hKLRG1.
Main Methods:
- Development of anti-hKLRG1 mAb (clone KLMab-1) using Cell-Based Immunization and Screening.
- Immunocytochemistry to evaluate mAb binding to exogenous hKLRG1 in CHO-K1 cells.
- Flow cytometry to confirm detection of endogenous hKLRG1 in human NK cells.
Main Results:
- The developed anti-hKLRG1 mAb (KLMab-1) and its recombinant version (recKLMab-1) successfully bound to exogenous hKLRG1.
- Both mAbs demonstrated the ability to detect endogenous hKLRG1 expressed in human NK cells.
- The study confirmed the availability of KLMab-1 and recKLMab-1 for immunocytochemistry applications.
Conclusions:
- KLMab-1 and recKLMab-1 are validated tools for detecting human KLRG1.
- These antibodies show potential for use in the diagnosis and immunotherapy of viral diseases and cancers.
- The findings support the utility of anti-KLRG1 antibodies in immunological research and clinical applications.
Abstract:
Immune checkpoint molecules have received attention as targets of cancer immunotherapy. Killer cell lectin-like receptor subfamily G member 1 (KLRG1) is one of the immune checkpoint molecules expressed in CD4+ T, CD8+ T, and natural killer (NK) cells. KLRG1 exhibits antiviral and antitumor immunity, and its expression in T and NK cells is upregulated by viral infectious diseases and some tumors. Thus, monoclonal antibodies (mAbs) for KLRG1 would be useful tools for the diagnosis and immunotherapy against viral infectious diseases and cancers. We have developed anti-human KLRG1 (hKLRG1) mAb (clone KLMab-1, mouse IgG1, kappa) by the Cell-Based Immunization and Screening method. We have also demonstrated that KLMab-1 recognizes both exogenous and endogenous hKLRG1 in flow cytometry. In this study, we first showed that KLMab-1 and its recombinant mAb (recKLMab-1) bound to exogenous hKLRG1 overexpressed in Chinese hamster ovary (CHO)-K1 cells, but not in parental CHO-K1 cells, in immunocytochemistry. We next showed that both mAbs detected endogenous hKLRG1 expressed in human NK cells. These results demonstrate that KLMab-1 and recKLMab-1 are available for immunocytochemistry.

