Granulocyte-Colony Stimulating Factor Nanocarriers for Stimulation of the Immune System (Part II): Dose-Dependent Biodistribution and In Vivo Antitumor Efficacy in Combination with Rituximab-Reference-Cited by-同舟云学术

Granulocyte-Colony Stimulating Factor Nanocarriers for Stimulation of the Immune System (Part II): Dose-Dependent Biodistribution and In Vivo Antitumor Efficacy in Combination with Rituximab

Published:2017-12-28 Issue:3 Volume:29 Page:804-812
ISSN:1043-1802
Container-title:Bioconjugate Chemistry
language:en
Short-container-title:Bioconjugate Chem.

Author:

Kryza David¹²^ORCID,De Crozals Gabriel³,Mathe Doriane⁴,Taleb Sidi-Boumedine Jacqueline¹,Janier Marc¹²,Chaix Carole³^ORCID,Dumontet Charles²⁴

Affiliation:

1. UNIV Lyon - Université Claude Bernard Lyon 1, LAGEP UMR 5007 CNRS, 69100 Villeurbanne, France

2. Hospices Civils de Lyon, 69437 Lyon, France

3. Institut des Sciences Analytiques, UMR 5280 CNRS/Université Claude Bernard Lyon 1/ENS de Lyon, 69100 Villeurbanne, France

4. Cancer Research Center of Lyon, INSERM 1052/CNRS 5286/University Claude Bernard Lyon 1, 69008 Lyon, France

Funder

Minist?re de l'Enseignement Sup?rieur et de la Recherche

Lyric

PULSALYS, SATT du site de Lyon St-Etienne

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Pharmaceutical Science,Pharmacology,Biomedical Engineering,Bioengineering,Biotechnology

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.bioconjchem.7b00606

Reference31 articles.

1. Increased natural killer cell expression of CD16, augmented binding and ADCC activity to rituximab among individuals expressing the FcγRIIIa-158 V/V and V/F polymorphism

2. Tuning of Natural Killer Cell Reactivity by NKp46 and Helios Calibrates T Cell Responses

3. Granulocyte-Macrophage Colony-Stimulating Factor Potentiates Rituximab in Patients With Relapsed Follicular Lymphoma: Results of a Phase II Study

4. Pegfilgrastim Enhances the Antitumor Effect of Therapeutic Monoclonal Antibodies

5. Granulocyte colony-stimulating factor stimulates recovery of granulocytes in patients receiving dose-intensive chemotherapy without bone marrow transplantation.

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