Jenna Geddes-Sweeney

ORCID: 0000-0003-2507-7314
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About
Contact & Profiles
Research Areas
  • Galectins and Cancer Biology
  • Cancer Mechanisms and Therapy
  • Signaling Pathways in Disease
  • Toxin Mechanisms and Immunotoxins
  • Glycosylation and Glycoproteins Research

Brigham and Women's Hospital
2015-2022

Harvard University
2022

T-cell immunoglobulin mucin family member 3 (Tim-3) is an immune checkpoint receptor that dampens effector functions and causes terminal exhaustion of cytotoxic T cells. Tim-3 inhibitors are under investigation in immuno-oncology (IO) trials, because blockade T-cell-Tim-3 enhances antitumor immunity. Here, we identify additional role for as a growth-suppressive intrinsic to melanoma Inhibition cell-Tim-3 promoted tumor growth both immunocompetent immunocompromised mice, while...

10.1158/0008-5472.can-22-0970 article EN Cancer Research 2022-08-18

<div>Abstract<p>T-cell immunoglobulin mucin family member 3 (Tim-3) is an immune checkpoint receptor that dampens effector functions and causes terminal exhaustion of cytotoxic T cells. Tim-3 inhibitors are under investigation in immuno-oncology (IO) trials, because blockade T-cell-Tim-3 enhances antitumor immunity. Here, we identify additional role for as a growth-suppressive intrinsic to melanoma Inhibition cell-Tim-3 promoted tumor growth both immunocompetent immunocompromised...

10.1158/0008-5472.c.6514280.v1 preprint EN 2023-03-31

<div>Abstract<p>T-cell immunoglobulin mucin family member 3 (Tim-3) is an immune checkpoint receptor that dampens effector functions and causes terminal exhaustion of cytotoxic T cells. Tim-3 inhibitors are under investigation in immuno-oncology (IO) trials, because blockade T-cell-Tim-3 enhances antitumor immunity. Here, we identify additional role for as a growth-suppressive intrinsic to melanoma Inhibition cell-Tim-3 promoted tumor growth both immunocompetent immunocompromised...

10.1158/0008-5472.c.6514280 preprint EN 2023-03-31
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