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Updated: Jan 30, 2026

High Yield Purification of Plasmodium falciparum Merozoites For Use in Opsonizing Antibody Assays
Published on: July 17, 2014
Antibody opsonization enhances MAIT cell responsiveness to bacteria via a TNF-dependent mechanism
Zoltán Bánki1, Lisette Krabbendam2, Dominik Klaver1
1Division of Virology, Medical University of Innsbruck, Innsbruck, Austria.
Abstract:
Mucosal-associated invariant T (MAIT) cells are an abundant human T-cell subset with antimicrobial properties. They can respond to bacteria presented via antigen-presenting cells (APCs) such as macrophages, which present bacterially derived ligands from the riboflavin synthesis pathway on MR1. Moreover, MAIT cells are also highly responsive to cytokines which enhance and even substitute for T-cell receptor-mediated signaling. The mechanisms leading to an efficient presentation of bacteria to MAIT cells by APCs have not been fully elucidated. Here, we showed that the monocytic cell line THP-1 and B cells activated MAIT cells differentially in response to Escherichia coli. THP-1 cells were generally more potent in inducing IFNγ and IFNγ/TNF production by MAIT cells. Furthermore, THP-1, but not B, cells produced TNF upon bacterial stimulation, which in turn supported IFNγ production by MAIT cells. Finally, we addressed the role of antibody-dependent opsonization of bacteria in the activation of MAIT cells using in vitro models. We found that opsonization had a substantial impact on downstream MAIT cell activation by monocytes. This was associated with enhanced activation of monocytes and increased TNF release. Importantly, this TNF acted in concert with other cytokines to drive MAIT cell activation. These data indicate both a significant interaction between adaptive and innate immunity in the response to bacteria, and an important role for TNF in MAIT cell triggering.
Insights
Mucosal-associated invariant T (MAIT) cells are activated by bacteria through antigen-presenting cells (APCs). Monocytes, especially when bacteria are opsonized, enhance MAIT cell responses, highlighting innate-adaptive immune interplay.
Area of Science:
- Immunology
- Microbiology
- Cellular Biology
Background:
- Mucosal-associated invariant T (MAIT) cells are a key T-cell subset with antimicrobial functions.
- MAIT cells recognize bacterial ligands presented by the MR1 molecule on antigen-presenting cells (APCs).
- Cytokines significantly influence MAIT cell activation, sometimes replacing T-cell receptor signaling.
Purpose of the Study:
- To investigate differential MAIT cell activation by distinct APCs in response to Escherichia coli.
- To elucidate the role of TNF in MAIT cell activation by APCs.
- To determine the impact of antibody-dependent opsonization on MAIT cell activation.
Main Methods:
- Comparative analysis of MAIT cell activation by THP-1 cells and B cells stimulated with E. coli.
- Measurement of cytokine production (IFNγ, TNF) by APCs and MAIT cells.
- In vitro modeling to assess the effect of antibody-dependent opsonization on monocyte and MAIT cell responses.
Main Results:
- THP-1 cells were more potent than B cells in inducing IFNγ and IFNγ/TNF production by MAIT cells.
- THP-1 cells produced TNF upon bacterial stimulation, which subsequently enhanced MAIT cell IFNγ production.
- Antibody-dependent opsonization significantly boosted MAIT cell activation by monocytes, correlating with increased monocyte activation and TNF release.
Conclusions:
- MAIT cell activation by bacteria involves differential responses mediated by various APCs.
- TNF plays a crucial role in MAIT cell activation, particularly when produced by monocytes.
- Antibody-dependent opsonization enhances innate immune cell activation, leading to robust MAIT cell responses, underscoring innate-adaptive immune synergy.
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