Frederick J. Kohlhapp

ORCID: 0009-0007-3132-5587
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About
Contact & Profiles
Research Areas
  • CAR-T cell therapy research
  • Immune Cell Function and Interaction
  • Immunotherapy and Immune Responses
  • Cancer Immunotherapy and Biomarkers
  • NF-κB Signaling Pathways
  • T-cell and B-cell Immunology
  • Virus-based gene therapy research
  • Viral gastroenteritis research and epidemiology
  • Synthesis and Biological Evaluation
  • Research in Cotton Cultivation
  • Viral Infectious Diseases and Gene Expression in Insects
  • Lymphoma Diagnosis and Treatment
  • RNA Interference and Gene Delivery
  • Neuroinflammation and Neurodegeneration Mechanisms
  • MicroRNA in disease regulation
  • Chronic Lymphocytic Leukemia Research
  • melanin and skin pigmentation
  • Cancer Research and Treatments
  • Heat shock proteins research
  • Immune cells in cancer
  • Magnesium in Health and Disease
  • Genomics, phytochemicals, and oxidative stress
  • Extracellular vesicles in disease
  • Pneumocystis jirovecii pneumonia detection and treatment
  • Advanced biosensing and bioanalysis techniques

AbbVie (United States)
2020-2024

Loyola University Chicago
2023

Rutgers, The State University of New Jersey
2015-2022

Rutgers Cancer Institute of New Jersey
2015-2017

Johnson University
2014-2017

Northwestern University
2013-2015

Rush University
2015

Rush University Medical Center
2014-2015

Rutgers Sexual and Reproductive Health and Rights
2015

University of Chicago
2010-2013

Significance Immunotherapy has revolutionized cancer treatment, yielding unprecedented long-term responses and survival. However, a significant proportion of patients remain refractory, which correlates with the absence immune-infiltrated (“hot”) tumors. Here, we observed that FDA-approved unadjuvanted seasonal influenza vaccines administered via intratumoral injection not only provide protection against active virus lung infection, but also reduce tumor growth by increasing antitumor CD8 +...

10.1073/pnas.1904022116 article EN cc-by Proceedings of the National Academy of Sciences 2019-12-30

Abstract The antiapoptotic protein BCL2 plays critical roles in regulating lymphocyte development and immune responses, has also been implicated tumorigenesis tumor survival. However, it is unknown whether for antitumor responses. We evaluated venetoclax, a selective small-molecule inhibitor of BCL2, would influence the activity checkpoint inhibitors (ICI). demonstrate mouse syngeneic models that venetoclax can augment efficacy ICIs accompanied by increase PD-1+ T effector memory cells....

10.1158/2159-8290.cd-19-0759 article EN Cancer Discovery 2020-09-04

Melanoma is one of the few types cancer with an increasing annual incidence. While a number immunotherapies for melanoma have been associated significant clinical benefit, including high-dose IL-2 and cytotoxic T lymphocyte antigen 4 (CTLA-4) blockade, response to either these single agents has limited 11-20% treated patients. Therefore, in this study, we sought test hypothesis that combination CTLA-4 blockade could mediate more profound therapeutic response.Here, B6 mice were challenged...

10.1186/s40425-015-0063-3 article EN cc-by-nc-nd Journal for ImmunoTherapy of Cancer 2015-05-13

d-Amino acid analogs of peptides and proteins are attractive for applications in biotechnology medicine due to their reduced proteolytic sensitivity. Here, we report that self-assembling peptide nanofibers composed d-amino acids act as immune adjuvants, investigate ability induce antibody responses comparison l-amino counterparts. The model antigenic OVA (chicken egg ovalbumin aa 323–339) from chicken ovalbumin, known elicit mice, was linked an l- or domain generate enantiomeric displaying...

10.1021/acsbiomaterials.5b00139 article EN ACS Biomaterials Science & Engineering 2015-06-05

Abstract The activated B cell (ABC) subset of diffuse large B-cell lymphoma (DLBCL) is characterized by chronic receptor signaling and associated with poor outcomes when treated standard therapy. In ABC-DLBCL, MALT1 a core enzyme that constitutively stimulation the or gain-of-function mutations in upstream components pathway, making it an attractive therapeutic target. We discovered novel small-molecule inhibitor, ABBV-MALT1, potently shuts down selectively ABC-DLBCL preclinical models...

10.1158/1535-7163.mct-23-0518 article EN cc-by-nc-nd Molecular Cancer Therapeutics 2024-03-20

In this study, we demonstrate that engagement of two different natural killer receptors (NKRs) can lead to contrasting effects in the development self-reactive CD8+T cells and autoimmune vitiligo. Specifically, using a mouse model, show CD8+T-cell targeting melanocyte antigen, tyrosinase-related protein-1 (TRP-1) combination with delivery NKG2D ligands (Rae-1ϵ or H60), results strong responses against TRP-1 contrast, CD48, ligand for NKR 2B4, leads reduced formation TRP-1-reactive decreased...

10.3109/08916934.2011.593599 article EN Autoimmunity 2011-09-13

A main goal of cancer immunology research is the formation Ag-specific memory T cell immunity capable activation upon tumor re-encounter. The requirements necessary to overcome inhibitory signals present in microenvironment and form such responses are unknown. In contrast previous studies targeting tumors expressing highly immunogenic model Ags, we demonstrate that alleviating tumor-induced suppression along with vaccination against authentic Ags during perioperative period provides...

10.4049/jimmunol.1002549 article EN The Journal of Immunology 2011-02-03

CD8 T cells play a critical role in immunity against intracellular pathogens and cancer. A primary objective of cell-based vaccine strategies is the induction durable effective immune responses. Achieving this goal involves more than simply boosting numbers responding cells. Of particular interest with polycytokine capability, specifically ability to co-produce IFNγ, TNFα IL-2. The presence these polycytokine-producing correlates strongly protection foreign Therefore, approaches capable...

10.1016/j.molimm.2022.12.013 article EN cc-by Molecular Immunology 2023-01-10

CD8(+) T cell responses have been shown to be regulated by dendritic cells (DCs) and CD4(+) cells, leading the tenet that play a passive role in their own differentiation. In contrast, using DNA vaccination model, separate events of from those priming, we demonstrate themselves, actively limit memory potential through cell-derived IFN-γ-dependent modification IL-12/IL-15Rα axis on DCs. Such cell-driven cytokine alterations result increased T-bet decreased Bcl-2 expression, thus progenitor...

10.4049/jimmunol.1101580 article EN The Journal of Immunology 2012-03-20
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