Targeting antigen-presenting cells by anti-PD-1 nanoparticles augments antitumor immunity. 2018

Farideh Ordikhani, and Mayuko Uehara, and Vivek Kasinath, and Li Dai, and Siawosh K Eskandari, and Baharak Bahmani, and Merve Yonar, and Jamil R Azzi, and Yousef Haik, and Peter T Sage, and George F Murphy, and Nasim Annabi, and Tobias Schatton, and Indira Guleria, and Reza Abdi
Transplantation Research Center, Renal Division, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.

Recent studies in cancer research have focused intensely on the antineoplastic effects of immune checkpoint inhibitors. While the development of these inhibitors has progressed successfully, strategies to further improve their efficacy and reduce their toxicity are still needed. We hypothesized that the delivery of anti-PD-1 antibody encapsulated in PLGA nanoparticles (anti-PD-1 NPs) to the spleen would improve the antitumor effect of this agent. Unexpectedly, we found that mice treated with a high dose of anti-PD-1 NPs exhibited significantly higher mortality compared with those treated with free anti-PD-1 antibody, due to the overactivation of T cells. Administration of anti-PD-1 NPs to splenectomized LT-α-/- mice, which lack both lymph nodes and spleen, resulted in a complete reversal of this increased mortality and revealed the importance of secondary lymphoid tissues in mediating anti-PD-1-associated toxicity. Attenuation of the anti-PD-1 NPs dosage prevented toxicity and significantly improved its antitumor effect in the B16-F10 murine melanoma model. Furthermore, we found that anti-PD-1 NPs undergo internalization by DCs in the spleen, leading to their maturation and the subsequent activation of T cells. Our findings provide important clues that can lead to the development of strategies to enhance the efficacy of immune checkpoint inhibitors.

UI MeSH Term Description Entries
D008233 Lymphotoxin-alpha A tumor necrosis factor family member that is released by activated LYMPHOCYTES. Soluble lymphotoxin is specific for TUMOR NECROSIS FACTOR RECEPTOR TYPE I; TUMOR NECROSIS FACTOR RECEPTOR TYPE II; and TUMOR NECROSIS FACTOR RECEPTOR SUPERFAMILY, MEMBER 14. Lymphotoxin-alpha can form a membrane-bound heterodimer with LYMPHOTOXIN-BETA that has specificity for the LYMPHOTOXIN BETA RECEPTOR. TNF Superfamily, Member 1,TNF-beta,Tumor Necrosis Factor Ligand Superfamily Member 1,Tumor Necrosis Factor-beta,Lymphotoxin,Lymphotoxin-alpha3,Soluble Lymphotoxin-alpha,alpha-Lymphotoxin,Lymphotoxin alpha,Lymphotoxin alpha3,Lymphotoxin-alpha, Soluble,Soluble Lymphotoxin alpha,Tumor Necrosis Factor beta,alpha Lymphotoxin
D009369 Neoplasms New abnormal growth of tissue. Malignant neoplasms show a greater degree of anaplasia and have the properties of invasion and metastasis, compared to benign neoplasms. Benign Neoplasm,Cancer,Malignant Neoplasm,Tumor,Tumors,Benign Neoplasms,Malignancy,Malignant Neoplasms,Neoplasia,Neoplasm,Neoplasms, Benign,Cancers,Malignancies,Neoplasias,Neoplasm, Benign,Neoplasm, Malignant,Neoplasms, Malignant
D003713 Dendritic Cells Specialized cells of the hematopoietic system that have branch-like extensions. They are found throughout the lymphatic system, and in non-lymphoid tissues such as SKIN and the epithelia of the intestinal, respiratory, and reproductive tracts. They trap and process ANTIGENS, and present them to T-CELLS, thereby stimulating CELL-MEDIATED IMMUNITY. They are different from the non-hematopoietic FOLLICULAR DENDRITIC CELLS, which have a similar morphology and immune system function, but with respect to humoral immunity (ANTIBODY PRODUCTION). Dendritic Cells, Interdigitating,Interdigitating Cells,Plasmacytoid Dendritic Cells,Veiled Cells,Dendritic Cells, Interstitial,Dendritic Cells, Plasmacytoid,Interdigitating Dendritic Cells,Interstitial Dendritic Cells,Cell, Dendritic,Cell, Interdigitating,Cell, Interdigitating Dendritic,Cell, Interstitial Dendritic,Cell, Plasmacytoid Dendritic,Cell, Veiled,Cells, Dendritic,Cells, Interdigitating,Cells, Interdigitating Dendritic,Cells, Interstitial Dendritic,Cells, Plasmacytoid Dendritic,Cells, Veiled,Dendritic Cell,Dendritic Cell, Interdigitating,Dendritic Cell, Interstitial,Dendritic Cell, Plasmacytoid,Interdigitating Cell,Interdigitating Dendritic Cell,Interstitial Dendritic Cell,Plasmacytoid Dendritic Cell,Veiled Cell
D004195 Disease Models, Animal Naturally-occurring or experimentally-induced animal diseases with pathological processes analogous to human diseases. Animal Disease Model,Animal Disease Models,Disease Model, Animal
D004305 Dose-Response Relationship, Drug The relationship between the dose of an administered drug and the response of the organism to the drug. Dose Response Relationship, Drug,Dose-Response Relationships, Drug,Drug Dose-Response Relationship,Drug Dose-Response Relationships,Relationship, Drug Dose-Response,Relationships, Drug Dose-Response
D004337 Drug Carriers Forms to which substances are incorporated to improve the delivery and the effectiveness of drugs. Drug carriers are used in drug-delivery systems such as the controlled-release technology to prolong in vivo drug actions, decrease drug metabolism, and reduce drug toxicity. Carriers are also used in designs to increase the effectiveness of drug delivery to the target sites of pharmacological actions. Liposomes, albumin microspheres, soluble synthetic polymers, DNA complexes, protein-drug conjugates, and carrier erythrocytes among others have been employed as biodegradable drug carriers. Drug Carrier
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000074322 Antineoplastic Agents, Immunological Antineoplastic agents containing immunological agents (e.g. MAbs). These pharmacologic preparations inhibit or prevent the proliferation of NEOPLASMS. Antineoplastic MAbs,Antineoplastics, Monoclonal Antibodies,Antineoplastics, Monoclonal Antibody,MAbs, Antineoplastic,Monoclonal Antibodies, Antineoplastic,Antibodies Antineoplastics, Monoclonal,Antineoplastic Monoclonal Antibodies,Immunological Antineoplastic Agents,Monoclonal Antibodies Antineoplastics,Monoclonal Antibody Antineoplastics
D000077182 Polylactic Acid-Polyglycolic Acid Copolymer A co-polymer that consists of varying ratios of polylactic acid and polyglycolic acid. It is used as a matrix for drug delivery and for BONE REGENERATION. PLGA Acid,LactoSorb,PL-PG Copolymer,PLG Polymer,PLGA Compound,Poly (D,L-lactic-co-glycolic Acid),Poly (Lactic-co-glycolic Acid) -,Poly(D,L-lactide-co-glycolide),Poly(DL-lactide-co-glycolic Acid),Poly(Glycolide-co-lactide),Poly(L-lactide)-co-glycolide,Poly(Lactic-co-glycolic Acid),Poly-L-lactic-polyglycolic Acid,Polylactic-co-glycolic Acid Copolymer,RG 502,Acid, PLGA,Acids, PLGA,Copolymer, PL-PG,Copolymer, Polylactic-co-glycolic Acid,Copolymers, PL-PG,Copolymers, Polylactic-co-glycolic Acid,PL PG Copolymer,PL-PG Copolymers,PLG Polymers,PLGA Acids,PLGA Compounds,Poly L lactic polyglycolic Acid,Poly-L-lactic-polyglycolic Acids,Polylactic Acid Polyglycolic Acid Copolymer,Polylactic co glycolic Acid Copolymer,Polylactic-co-glycolic Acid Copolymers,Polymer, PLG,Polymers, PLG

Related Publications

Farideh Ordikhani, and Mayuko Uehara, and Vivek Kasinath, and Li Dai, and Siawosh K Eskandari, and Baharak Bahmani, and Merve Yonar, and Jamil R Azzi, and Yousef Haik, and Peter T Sage, and George F Murphy, and Nasim Annabi, and Tobias Schatton, and Indira Guleria, and Reza Abdi
November 2023, The Journal of clinical investigation,
Farideh Ordikhani, and Mayuko Uehara, and Vivek Kasinath, and Li Dai, and Siawosh K Eskandari, and Baharak Bahmani, and Merve Yonar, and Jamil R Azzi, and Yousef Haik, and Peter T Sage, and George F Murphy, and Nasim Annabi, and Tobias Schatton, and Indira Guleria, and Reza Abdi
January 2015, Future oncology (London, England),
Farideh Ordikhani, and Mayuko Uehara, and Vivek Kasinath, and Li Dai, and Siawosh K Eskandari, and Baharak Bahmani, and Merve Yonar, and Jamil R Azzi, and Yousef Haik, and Peter T Sage, and George F Murphy, and Nasim Annabi, and Tobias Schatton, and Indira Guleria, and Reza Abdi
June 2020, Cancer research,
Farideh Ordikhani, and Mayuko Uehara, and Vivek Kasinath, and Li Dai, and Siawosh K Eskandari, and Baharak Bahmani, and Merve Yonar, and Jamil R Azzi, and Yousef Haik, and Peter T Sage, and George F Murphy, and Nasim Annabi, and Tobias Schatton, and Indira Guleria, and Reza Abdi
January 2020, Clinical cancer research : an official journal of the American Association for Cancer Research,
Farideh Ordikhani, and Mayuko Uehara, and Vivek Kasinath, and Li Dai, and Siawosh K Eskandari, and Baharak Bahmani, and Merve Yonar, and Jamil R Azzi, and Yousef Haik, and Peter T Sage, and George F Murphy, and Nasim Annabi, and Tobias Schatton, and Indira Guleria, and Reza Abdi
June 2017, Oncotarget,
Farideh Ordikhani, and Mayuko Uehara, and Vivek Kasinath, and Li Dai, and Siawosh K Eskandari, and Baharak Bahmani, and Merve Yonar, and Jamil R Azzi, and Yousef Haik, and Peter T Sage, and George F Murphy, and Nasim Annabi, and Tobias Schatton, and Indira Guleria, and Reza Abdi
January 2020, Advanced science (Weinheim, Baden-Wurttemberg, Germany),
Farideh Ordikhani, and Mayuko Uehara, and Vivek Kasinath, and Li Dai, and Siawosh K Eskandari, and Baharak Bahmani, and Merve Yonar, and Jamil R Azzi, and Yousef Haik, and Peter T Sage, and George F Murphy, and Nasim Annabi, and Tobias Schatton, and Indira Guleria, and Reza Abdi
August 2023, Gut,
Farideh Ordikhani, and Mayuko Uehara, and Vivek Kasinath, and Li Dai, and Siawosh K Eskandari, and Baharak Bahmani, and Merve Yonar, and Jamil R Azzi, and Yousef Haik, and Peter T Sage, and George F Murphy, and Nasim Annabi, and Tobias Schatton, and Indira Guleria, and Reza Abdi
November 2019, Journal for immunotherapy of cancer,
Farideh Ordikhani, and Mayuko Uehara, and Vivek Kasinath, and Li Dai, and Siawosh K Eskandari, and Baharak Bahmani, and Merve Yonar, and Jamil R Azzi, and Yousef Haik, and Peter T Sage, and George F Murphy, and Nasim Annabi, and Tobias Schatton, and Indira Guleria, and Reza Abdi
February 2020, Journal of the American Chemical Society,
Farideh Ordikhani, and Mayuko Uehara, and Vivek Kasinath, and Li Dai, and Siawosh K Eskandari, and Baharak Bahmani, and Merve Yonar, and Jamil R Azzi, and Yousef Haik, and Peter T Sage, and George F Murphy, and Nasim Annabi, and Tobias Schatton, and Indira Guleria, and Reza Abdi
January 2001, Microbes and infection,
Copied contents to your clipboard!