Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters










Database
Language
Publication year range
1.
J Exp Clin Cancer Res ; 41(1): 131, 2022 Apr 07.
Article in English | MEDLINE | ID: mdl-35392965

ABSTRACT

BACKGROUND: Hypoxia is a hallmark of the tumor microenvironment (TME) and in addition to altering metabolism in cancer cells, it transforms tumor-associated stromal cells. Within the tumor stromal cell compartment, tumor-associated macrophages (TAMs) provide potent pro-tumoral support. However, TAMs can also be harnessed to destroy tumor cells by monoclonal antibody (mAb) immunotherapy, through antibody dependent cellular phagocytosis (ADCP). This is mediated via antibody-binding activating Fc gamma receptors (FcγR) and impaired by the single inhibitory FcγR, FcγRIIb. METHODS: We applied a multi-OMIC approach coupled with in vitro functional assays and murine tumor models to assess the effects of hypoxia inducible factor (HIF) activation on mAb mediated depletion of human and murine cancer cells. For mechanistic assessments, siRNA-mediated gene silencing, Western blotting and chromatin immune precipitation were utilized to assess the impact of identified regulators on FCGR2B gene transcription. RESULTS: We report that TAMs are FcγRIIbbright relative to healthy tissue counterparts and under hypoxic conditions, mononuclear phagocytes markedly upregulate FcγRIIb. This enhanced FcγRIIb expression is transcriptionally driven through HIFs and Activator protein 1 (AP-1). Importantly, this phenotype reduces the ability of macrophages to eliminate anti-CD20 monoclonal antibody (mAb) opsonized human chronic lymphocytic leukemia cells in vitro and EL4 lymphoma cells in vivo in human FcγRIIb+/+ transgenic mice. Furthermore, post-HIF activation, mAb mediated blockade of FcγRIIb can partially restore phagocytic function in human monocytes. CONCLUSION: Our findings provide a detailed molecular and cellular basis for hypoxia driven resistance to antitumor mAb immunotherapy, unveiling a hitherto unexplored aspect of the TME. These findings provide a mechanistic rationale for the modulation of FcγRIIb expression or its blockade as a promising strategy to enhance approved and novel mAb immunotherapies.


Subject(s)
Leukemia, Lymphocytic, Chronic, B-Cell , Receptors, IgG , Animals , Antibodies, Monoclonal/pharmacology , Humans , Hypoxia/metabolism , Immunotherapy , Leukemia, Lymphocytic, Chronic, B-Cell/metabolism , Macrophages/metabolism , Mice , Receptors, IgG/genetics , Receptors, IgG/metabolism , Tumor Microenvironment
2.
Food Cult Soc ; 16(1): 65-84, 2013 Mar.
Article in English | MEDLINE | ID: mdl-25414598

ABSTRACT

Accurate measurement of household food security is essential to generate adequate information on the proportion of households experiencing food insecurity, especially in areas or regions vulnerable to food shortages and famine. This manuscript offers a methodological examination of three commonly used indicators of household food security - experience of hunger, dietary diversity, and coping strategies. Making use of data from the Agincourt Health and Demographic Surveillance Site in rural South Africa, we examine the association between the indicators themselves to improve understanding of the different insight offered by each food security "lens." We also examine how the choice of indicator shapes the profile of vulnerable households, with results suggesting that dietary diversity scores may not adequately capture broader food insecurity. Concluding discussion explores programmatic and policy implications as related to methodological choices.

SELECTION OF CITATIONS
SEARCH DETAIL
...