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The Society for Immunotherapy of Cancer statement on best practices for multiplex immunohistochemistry (IHC) and immunofluorescence (IF) staining and validation.
Taube, Janis M; Akturk, Guray; Angelo, Michael; Engle, Elizabeth L; Gnjatic, Sacha; Greenbaum, Shirley; Greenwald, Noah F; Hedvat, Cyrus V; Hollmann, Travis J; Juco, Jonathan; Parra, Edwin R; Rebelatto, Marlon C; Rimm, David L; Rodriguez-Canales, Jaime; Schalper, Kurt A; Stack, Edward C; Ferreira, Cláudia S; Korski, Konstanty; Lako, Ana; Rodig, Scott J; Schenck, Emanuel; Steele, Keith E; Surace, Michael J; Tetzlaff, Michael T; von Loga, Katharina; Wistuba, Ignacio I; Bifulco, Carlo B.
Afiliação
  • Taube JM; Department of Dermatology, Johns Hopkins School of Medicine, Bloomberg~Kimmel Institute for Cancer Immunotherapy, Baltimore, Maryland, USA jtaube1@jhmi.edu.
  • Akturk G; Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, New York City, USA.
  • Angelo M; Department of Pathology, Stanford University School of Medicine, Palo Alto, California, USA.
  • Engle EL; Department of Dermatology, Johns Hopkins School of Medicine, Bloomberg~Kimmel Institute for Cancer Immunotherapy, Baltimore, Maryland, USA.
  • Gnjatic S; Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, New York City, USA.
  • Greenbaum S; Department of Pathology, Stanford University School of Medicine, Palo Alto, California, USA.
  • Greenwald NF; Department of Pathology, Stanford University School of Medicine, Palo Alto, California, USA.
  • Hedvat CV; Cancer Biology Program, Stanford University School of Medicine, Palo Alto, California, USA.
  • Hollmann TJ; Bristol-Myers Squibb, New York, New York City, USA.
  • Juco J; Dermatopathology, Memorial Sloan-Kettering Cancer Center, New York, New York, USA.
  • Parra ER; Merck & Co Inc, Kenilworth, New Jersey, USA.
  • Rebelatto MC; Department of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Rimm DL; AstraZeneca, Gaithersburg, Maryland, USA.
  • Rodriguez-Canales J; Department of Pathology, Yale University School of Medicine, New Haven, Connecticut, USA.
  • Schalper KA; AstraZeneca, Gaithersburg, Maryland, USA.
  • Stack EC; Department of Pathology, Yale University School of Medicine, New Haven, Connecticut, USA.
  • Ferreira CS; Jounce Therapeutics Inc, Cambridge, Massachusetts, USA.
  • Korski K; Pharma Research and Early Development (pRED), Roche Innovation Center Munich, Penzberg, Germany.
  • Lako A; Pharma Research and Early Development (pRED), Roche Innovation Center Munich, Penzberg, Germany.
  • Rodig SJ; Dana-Farber/Brigham and Women's Cancer Center, Boston, Massachusetts, USA.
  • Schenck E; Harvard Medical School, Boston, Massachusetts, USA.
  • Steele KE; Dana-Farber/Brigham and Women's Cancer Center, Boston, Massachusetts, USA.
  • Surace MJ; Harvard Medical School, Boston, Massachusetts, USA.
  • Tetzlaff MT; AstraZeneca, Gaithersburg, Maryland, USA.
  • von Loga K; AstraZeneca, Gaithersburg, Maryland, USA.
  • Wistuba II; AstraZeneca, Gaithersburg, Maryland, USA.
  • Bifulco CB; Department of Translational Molecular Pathology, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
J Immunother Cancer ; 8(1)2020 05.
Article em En | MEDLINE | ID: mdl-32414858
ABSTRACT

OBJECTIVES:

The interaction between the immune system and tumor cells is an important feature for the prognosis and treatment of cancer. Multiplex immunohistochemistry (mIHC) and multiplex immunofluorescence (mIF) analyses are emerging technologies that can be used to help quantify immune cell subsets, their functional state, and their spatial arrangement within the tumor microenvironment.

METHODS:

The Society for Immunotherapy of Cancer (SITC) convened a task force of pathologists and laboratory leaders from academic centers as well as experts from pharmaceutical and diagnostic companies to develop best practice guidelines for the optimization and validation of mIHC/mIF assays across platforms.

RESULTS:

Representative outputs and the advantages and disadvantages of mIHC/mIF approaches, such as multiplexed chromogenic IHC, multiplexed immunohistochemical consecutive staining on single slide, mIF (including multispectral approaches), tissue-based mass spectrometry, and digital spatial profiling are discussed.

CONCLUSIONS:

mIHC/mIF technologies are becoming standard tools for biomarker studies and are likely to enter routine clinical practice in the near future. Careful assay optimization and validation will help ensure outputs are robust and comparable across laboratories as well as potentially across mIHC/mIF platforms. Quantitative image analysis of mIHC/mIF output and data management considerations will be addressed in a complementary manuscript from this task force.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Coloração e Rotulagem / Imuno-Histoquímica / Imunofluorescência / Microambiente Tumoral / Imunoterapia Limite: Humans Idioma: En Revista: J Immunother Cancer Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Coloração e Rotulagem / Imuno-Histoquímica / Imunofluorescência / Microambiente Tumoral / Imunoterapia Limite: Humans Idioma: En Revista: J Immunother Cancer Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos
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