Immune co-culture cell microarray - a feasible tool for high-throughput functional investigation of lymphocyte-cancer interactions.

Immunotherapy functional protein expression immunological cytotoxicity test melanoma omics validation

Journal

Oncoimmunology
ISSN: 2162-4011
Titre abrégé: Oncoimmunology
Pays: United States
ID NLM: 101570526

Informations de publication

Date de publication:
2020
Historique:
received: 28 09 2019
revised: 09 01 2020
accepted: 09 01 2020
entrez: 7 5 2020
pubmed: 7 5 2020
medline: 7 5 2020
Statut: epublish

Résumé

Omics analyses often result in dozens to hundreds of potential targets, requiring validation for their biological relevance. Current high-throughput functional investigation methods are frequently labor-intensive, expensive, and display low reproducibility. The Immune Co-Culture Cell Microarray (ICCM) is a formalin-fixed paraffin-embedded cell block microarray based on co-cultures of patient-derived tumor-infiltrating lymphocytes and their autologous melanoma cells. Each ICCM slide represents the same experiment and can be stained using standard immunohistochemistry and immunofluorescence techniques. Functional dynamics assessment of both proteins and microRNAs using ICCM stained slides demonstrated similar findings to flow cytometry assays and to previously published patient-derived biopsy reports.

Identifiants

pubmed: 32373399
doi: 10.1080/2162402X.2020.1741267
pii: 1741267
pmc: PMC7194292
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Pagination

1741267

Informations de copyright

© 2020 The Author(s). Published with license by Taylor & Francis Group, LLC.

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Auteurs

Erez Nissim Baruch (EN)

Department of Clinical Immunology and Microbiology, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
The Ella Lemelbaum Institute for Immuno-Oncology, Sheba Medical Center, Tel-HaShomer, Israel.

Rona Ortenberg (R)

The Ella Lemelbaum Institute for Immuno-Oncology, Sheba Medical Center, Tel-HaShomer, Israel.

Camila Avivi (C)

Pathological Institute, Sheba Medical Center, Tel-HaShomer; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.

Liat Anafi (L)

Pathological Institute, Sheba Medical Center, Tel-HaShomer; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.

Daniela Dick-Necula (D)

Pathological Institute, Sheba Medical Center, Tel-HaShomer; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.

Chani Stossel (C)

Department of Clinical Immunology and Microbiology, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
The Ella Lemelbaum Institute for Immuno-Oncology, Sheba Medical Center, Tel-HaShomer, Israel.

Yonatan Moshkovits (Y)

School of Of Medicine, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Orit Itzhaki (O)

The Ella Lemelbaum Institute for Immuno-Oncology, Sheba Medical Center, Tel-HaShomer, Israel.

Michal Judith Besser (MJ)

Department of Clinical Immunology and Microbiology, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
The Ella Lemelbaum Institute for Immuno-Oncology, Sheba Medical Center, Tel-HaShomer, Israel.

Jacob Schachter (J)

The Ella Lemelbaum Institute for Immuno-Oncology, Sheba Medical Center, Tel-HaShomer, Israel.
School of Of Medicine, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Iris Barshack (I)

Pathological Institute, Sheba Medical Center, Tel-HaShomer; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
School of Of Medicine, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Gal Markel (G)

Department of Clinical Immunology and Microbiology, Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
The Ella Lemelbaum Institute for Immuno-Oncology, Sheba Medical Center, Tel-HaShomer, Israel.
Talpiot Medical Leadership Program, Sheba Medical Center, Tel HaShomer, Israel.

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Classifications MeSH