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Biology subjects

Jugler, C.

Publications and source records attributed to Jugler, C..

2 recordsLinked to original sources

Cytotoxic CD4+ exTregs expressing KLRG1 retain immunosuppressive function in cancer

The role of cytotoxic CD4+ T cells in cancer remains controversial, with both pro- and anti-tumor functionality described. Based on a prior observation that putatively cytotoxic KLRG1+ FoxP3- conventional T cells (Tconv) associated with tumor progression, we deeply investigated the phenotype and function of KLRG1+ Tconv in multiple murine tumor models and in human clear cell renal cell carcinoma (ccRCC) specimens. We found KLRG1+ Tconv have a conserved, highly activated, terminally differentiated phenotype across species. In murine tumors, KLRG1+ Tconv resemble tumor-infiltrating regulatory T cells (Tregs) at both transcriptional and proteomic levels, upregulating a spectrum of exhaustion-related checkpoint receptors, producing IL-10 and granzyme B (GzmB), and silencing expression of IFN{gamma} and TNF. Functionally, KLRG1+ Tconv exhibited immunosuppressive function in ex vivo assays. Using an in vivo Treg fate mapping approach in tumor-bearing mice, we found a subset of KLRG1+ Tconv are derived from Tregs that have lost FoxP3 protein expression. Ex vivo functional assays demonstrated the exTreg component of the KLRG1+ Tconv compartment is responsible for IL-10 production and reduced pro-inflammatory cytokine expression. In treatment studies, we found that KLRG1-targeted antibody-mediated depletion was more efficient than anti-KLRG1 blockade at slowing tumor growth and improving survival, with responses associating with depletion of intratumoral KLRG1+ Tconv and Tregs. In sum, our study discovered a novel conserved pathway of CD4+ T cell plasticity, wherein intratumoral, cytotoxic KLRG1+ CD4+ Tconv cells can be derived from Tregs and maintain immunosuppressive function, despite loss of FoxP3, and that KLRG1-targeted depletion may outperform KLRG1 blockade as an immunotherapeutic strategy in cancer.

immunology↗

Humanization and Expression of IgG and IgM Antibodies in Plants as Potential Diagnostic Reagents for Valley Fever

Monoclonal antibodies (mAbs) are important proteins used in many life science applications, from diagnostics to therapeutics. High demand for mAbs for different applications urges the development of rapid and reliable recombinant production platforms. Plants provide a quick and inexpensive system for producing recombinant mAbs. Moreover, when paired with an established platform for mAb discovery, plants can easily be tailored to produce mAbs of different isotypes against the same target. Here, we demonstrate that a hybridoma-generated mouse mAb against chitinase 1 (CTS1), an antigen from Coccidioides spp., can be biologically engineered for use with serologic diagnostic test kits for coccidioidomycosis (Valley Fever) using plant expression. The original mouse IgG was modified and recombinantly produced in plants as IgG and IgM isotypes with human kappa, gamma, and mu constant regions. The two mAb isotypes produced in plants were shown to maintain target antigen recognition to CTS1 using similar reagents as the Food and Drug Administration (FDA)-approved Valley Fever diagnostic kits. As none of the currently approved kits provide antibody dilution controls, humanization of antibodies that bind to CTS1, a major component of the diagnostic antigen preparation, may provide a solution to the lack of consistently reactive antibody controls for Valley Fever diagnosis. Furthermore, our work provides a foundation for reproducible and consistent production of recombinant mAbs engineered to have a specific isotype for use in diagnostic assays.

immunology↗