Lana Chisholm

ORCID: 0000-0003-2102-9083
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About
Contact & Profiles
Research Areas
  • Cancer Immunotherapy and Biomarkers
  • Immune Cell Function and Interaction
  • Immunotherapy and Immune Responses
  • T-cell and B-cell Immunology
  • Immune cells in cancer
  • Children's Physical and Motor Development
  • Obesity, Physical Activity, Diet
  • Immune Response and Inflammation
  • Physical Activity and Health
  • Sirtuins and Resveratrol in Medicine
  • Prostate Cancer Treatment and Research
  • Tryptophan and brain disorders
  • Gut microbiota and health

Auckland University of Technology
2022

Providence Portland Medical Center
2012-2014

Oregon Health & Science University
2013

Vaccine and Gene Therapy Institute
2013

Providence Regional Medical Center Everett
2013

Abstract OX40 is a potent costimulatory receptor that can potentiate T-cell signaling on the surface of T lymphocytes, leading to their activation by specifically recognized antigen. In particular, engagement ligands present dendritic cells dramatically increases proliferation, effector function, and survival cells. Preclinical studies have shown agonists increase antitumor immunity improve tumor-free survival. this study, we performed phase I clinical trial using mouse monoclonal antibody...

10.1158/0008-5472.can-12-4174 article EN Cancer Research 2013-11-01

This article reports the methods and findings for Aotearoa New Zealand's 2022 Report Card on Physical Activity Children Youth indicators, inequities within these indicators.Grades were assigned to indicators using Active Healthy Kids Global Alliance criteria depending data availability, reported based gender, ethnicity, disability status, area-level socioeconomic deprivation, urbanicity, school year. Two additional included in this report card: Sleep, literacy.Grades as follows: Overall...

10.1016/j.jesf.2022.10.009 article EN cc-by-nc-nd Journal of Exercise Science & Fitness 2022-11-04

<h3>Background</h3> We examined the phenotype and function of lymphocytes collected from peripheral blood (PBL) tumor (TIL) patients with two different solid malignancies: colorectal cancer liver metastases (CRLM) ovarian (OVC). <h3>Methods</h3> Tumor corresponding were 16 CRLM 22 OVC patients; immediately following resection they processed analyzed using a multi-color flow cytometry panel. Cytokine mRNA purified PBL TIL CD4<sup>+</sup> T cells also by qPCR. <h3>Results</h3> Overall, we...

10.1186/s40425-014-0038-9 article EN cc-by-nc-nd Journal for ImmunoTherapy of Cancer 2014-11-14

Meeting abstracts OX40, a member of the Tumor Necrosis Factor Receptor superfamily is potent co-stimulatory molecule. OX40 engagement increases T cell proliferation, effector function and survival. Pre-clinical studies have shown that agonist synergizes with radiation cyclophosphamide to

10.1186/2051-1426-1-s1-p255 article EN cc-by Journal for ImmunoTherapy of Cancer 2013-11-01

<h3>Background</h3> We examined the phenotype and function of lymphocytes collected from peripheral blood (PBL) tumor (TIL) patients with two different solid malignancies: colorectal cancer liver metastases (CRLM) ovarian (OVC). <h3>Methods</h3> Tumor corresponding were 16 CRLM 22 OVC patients; immediately following resection they processed analyzed using a multi-color flow cytometry panel. Cytokine mRNA purified PBL TIL CD4<sup>+</sup> T cells also by qPCR. <h3>Results</h3> Overall, we...

10.1186/preaccept-2094627261309808 article EN cc-by-nc-nd Journal for ImmunoTherapy of Cancer 2014-01-01

Abstract Characterizing TIL composition allows monitoring of immunotherapies and can be a prognostic factor for clinical outcome. Here we analyze the phenotype function lymphocytes collected from peripheral blood tumor infiltrating lymphocytes, immediately following resection, 15 patients with colorectal cancer liver metastases (CRLM) 21 ovarian primary tumors (OVC). Samples were analyzed using multi-color flow panel by qPCR cytokine production. The percentage different lymphocyte...

10.4049/jimmunol.190.supp.170.18 article EN The Journal of Immunology 2013-05-01

&lt;p&gt;PDF file - 198K, Figure 1. Characterization of the anti-OX40 mAb (9B12). 2. Total peripheral lymphocyte counts. 3. Pharmacokinetics CD134 (anti-OX40) in patients. 4. Direct ex vivo detection murine bound to T cells treated 5. Regression a pulmonary metastasis patient with renal carcinoma enrolled cohort 6. Changes Ki-67 expression within CD4+ and CD8+ cell subsets examined over time after from patients cohorts 1 7. Increased proliferation Foxp3- correlates decrease or stabilization...

10.1158/0008-5472.22396172 preprint EN cc-by 2023-03-30

&lt;p&gt;PDF file - 198K, Figure 1. Characterization of the anti-OX40 mAb (9B12). 2. Total peripheral lymphocyte counts. 3. Pharmacokinetics CD134 (anti-OX40) in patients. 4. Direct ex vivo detection murine bound to T cells treated 5. Regression a pulmonary metastasis patient with renal carcinoma enrolled cohort 6. Changes Ki-67 expression within CD4+ and CD8+ cell subsets examined over time after from patients cohorts 1 7. Increased proliferation Foxp3- correlates decrease or stabilization...

10.1158/0008-5472.22396172.v1 preprint EN cc-by 2023-03-30

&lt;div&gt;Abstract&lt;p&gt;OX40 is a potent costimulatory receptor that can potentiate T-cell signaling on the surface of T lymphocytes, leading to their activation by specifically recognized antigen. In particular, OX40 engagement ligands present dendritic cells dramatically increases proliferation, effector function, and survival cells. Preclinical studies have shown agonists increase antitumor immunity improve tumor-free survival. this study, we performed phase I clinical trial using...

10.1158/0008-5472.c.6504491 preprint EN 2023-03-30

&lt;div&gt;Abstract&lt;p&gt;OX40 is a potent costimulatory receptor that can potentiate T-cell signaling on the surface of T lymphocytes, leading to their activation by specifically recognized antigen. In particular, OX40 engagement ligands present dendritic cells dramatically increases proliferation, effector function, and survival cells. Preclinical studies have shown agonists increase antitumor immunity improve tumor-free survival. this study, we performed phase I clinical trial using...

10.1158/0008-5472.c.6504491.v1 preprint EN 2023-03-30

Abstract Age-related defects accumulate in both the innate and adaptive arms of immunity to generate a state immune deficiency. Our laboratory has previously shown decrease responses aged mice compared younger context OX40 costimulation. This loss during aging underscores need for simple approaches boost older individuals. We hypothesize that activation or blockade CTLA-4 can be restored and/or maintained through caloric restriction (CR) dietary supplementation with CR mimetic. Two regimens...

10.4049/jimmunol.188.supp.47.14 article EN The Journal of Immunology 2012-05-01
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