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Antitumor efficacy of multi-target in situ vaccinations with CpG oligodeoxynucleotides, anti-OX40, anti-PD1 antibodies, and aptamers. / Proskurina, Anastasia S.; Рузанова, Вера Сергеевна; Риттер, Генрих Сергеевич и др.

в: Journal of Biomedical Research, Том 37, № 3, 2023, стр. 194-212.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

Harvard

Proskurina, AS, Рузанова, ВС, Риттер, ГС, Ефремов, ЯР, Mustafin, ZS, Лашин, СА, Буракова, ЕА, Фокина, АА, Zatsepin, TS, Стеценко, ДА, Леплина, ОЮ, Останин, АА, Черных, ЕР & Bogachev, SS 2023, 'Antitumor efficacy of multi-target in situ vaccinations with CpG oligodeoxynucleotides, anti-OX40, anti-PD1 antibodies, and aptamers', Journal of Biomedical Research, Том. 37, № 3, стр. 194-212. https://doi.org/10.7555/JBR.36.20220052

APA

Proskurina, A. S., Рузанова, В. С., Риттер, Г. С., Ефремов, Я. Р., Mustafin, Z. S., Лашин, С. А., Буракова, Е. А., Фокина, А. А., Zatsepin, T. S., Стеценко, Д. А., Леплина, О. Ю., Останин, А. А., Черных, Е. Р., & Bogachev, S. S. (2023). Antitumor efficacy of multi-target in situ vaccinations with CpG oligodeoxynucleotides, anti-OX40, anti-PD1 antibodies, and aptamers. Journal of Biomedical Research, 37(3), 194-212. https://doi.org/10.7555/JBR.36.20220052

Vancouver

Proskurina AS, Рузанова ВС, Риттер ГС, Ефремов ЯР, Mustafin ZS, Лашин СА и др. Antitumor efficacy of multi-target in situ vaccinations with CpG oligodeoxynucleotides, anti-OX40, anti-PD1 antibodies, and aptamers. Journal of Biomedical Research. 2023;37(3):194-212. Epub 2022 нояб. 28. doi: 10.7555/JBR.36.20220052

Author

Proskurina, Anastasia S. ; Рузанова, Вера Сергеевна ; Риттер, Генрих Сергеевич и др. / Antitumor efficacy of multi-target in situ vaccinations with CpG oligodeoxynucleotides, anti-OX40, anti-PD1 antibodies, and aptamers. в: Journal of Biomedical Research. 2023 ; Том 37, № 3. стр. 194-212.

BibTeX

@article{5a3fcf8b868b486090372f7a16eda8e8,
title = "Antitumor efficacy of multi-target in situ vaccinations with CpG oligodeoxynucleotides, anti-OX40, anti-PD1 antibodies, and aptamers",
abstract = "To overcome immune tolerance to cancer, the immune system needs to be exposed to a multi-target action intervention. Here, we investigated the activating effect of CpG oligodeoxynucleotides, mesyl phosphoramidate CpG oligodeoxynucleotides, anti-OX40 antibodies, and OX40 RNA aptamers on major populations of immunocompetent cells ex vivo. Comparative analysis of the antitumor effects of in situ vaccination with CpG oligodeoxynucleotides and anti-OX40 antibodies, as well as several other combinations such as mesyl phosphoramidate CpG oligodeoxynucleotides and OX40 RNA aptamers, were conducted. Antibodies against programmed death 1 (PD1) checkpoint inhibitors or corresponding PD1 DNA aptamers were also added to vaccination regimens for analytical purposes. Four scenarios were considered: a weakly immunogenic Krebs-2 carcinoma grafted in CBA mice; a moderately immunogenic Lewis carcinoma grafted in C57Black mice; and an immunogenic A20 B cell lymphoma or an Erlich carcinoma, grafted in BALB/c mice. Adding anti-PD1 antibodies (CpG+αOX40+αPD1) to in situ vaccinations boosts the antitumor effect. When used instead of antibodies, aptamers also possess antitumor activity, although this effect was less pronounced. The strongest effect across all the tumors was observed in highly immunogenic A20 B cell lymphoma and Erlich carcinoma.",
keywords = "immunogenicity, Krebs-2 carcinoma, Lewis carcinoma, Erlich carcinoma, A20 B cell lymphoma, mesyl phosphoramidate",
author = "Proskurina, {Anastasia S.} and Рузанова, {Вера Сергеевна} and Риттер, {Генрих Сергеевич} and Ефремов, {Ярослав Рейнгольдович} and Mustafin, {Zakhar Sergeevich} and Лашин, {Сергей Александрович} and Буракова, {Екатерина Анатольевна} and Фокина, {Алеся Анатольевна} and Zatsepin, {Timofei S.} and Стеценко, {Дмитрий Александрович} and Леплина, {Ольга Юрьевна} and Останин, {Александр Анатольевич} and Черных, {Елена Рэмовна} and Bogachev, {Sergey S.}",
note = "Fundings: The work was supported by the Russian Ministry of Science and High Education via the Institute of Cytology and Genetics (State Budget Project No. FWNR-2022-0016) and Russian Foundation for Basic Research (Grant No. 18-29-09045).",
year = "2023",
doi = "10.7555/JBR.36.20220052",
language = "English",
volume = "37",
pages = "194--212",
journal = "Journal of Biomedical Research",
issn = "1674-8301",
publisher = "Nanjing Medical University",
number = "3",

}

RIS

TY - JOUR

T1 - Antitumor efficacy of multi-target in situ vaccinations with CpG oligodeoxynucleotides, anti-OX40, anti-PD1 antibodies, and aptamers

AU - Proskurina, Anastasia S.

AU - Рузанова, Вера Сергеевна

AU - Риттер, Генрих Сергеевич

AU - Ефремов, Ярослав Рейнгольдович

AU - Mustafin, Zakhar Sergeevich

AU - Лашин, Сергей Александрович

AU - Буракова, Екатерина Анатольевна

AU - Фокина, Алеся Анатольевна

AU - Zatsepin, Timofei S.

AU - Стеценко, Дмитрий Александрович

AU - Леплина, Ольга Юрьевна

AU - Останин, Александр Анатольевич

AU - Черных, Елена Рэмовна

AU - Bogachev, Sergey S.

N1 - Fundings: The work was supported by the Russian Ministry of Science and High Education via the Institute of Cytology and Genetics (State Budget Project No. FWNR-2022-0016) and Russian Foundation for Basic Research (Grant No. 18-29-09045).

PY - 2023

Y1 - 2023

N2 - To overcome immune tolerance to cancer, the immune system needs to be exposed to a multi-target action intervention. Here, we investigated the activating effect of CpG oligodeoxynucleotides, mesyl phosphoramidate CpG oligodeoxynucleotides, anti-OX40 antibodies, and OX40 RNA aptamers on major populations of immunocompetent cells ex vivo. Comparative analysis of the antitumor effects of in situ vaccination with CpG oligodeoxynucleotides and anti-OX40 antibodies, as well as several other combinations such as mesyl phosphoramidate CpG oligodeoxynucleotides and OX40 RNA aptamers, were conducted. Antibodies against programmed death 1 (PD1) checkpoint inhibitors or corresponding PD1 DNA aptamers were also added to vaccination regimens for analytical purposes. Four scenarios were considered: a weakly immunogenic Krebs-2 carcinoma grafted in CBA mice; a moderately immunogenic Lewis carcinoma grafted in C57Black mice; and an immunogenic A20 B cell lymphoma or an Erlich carcinoma, grafted in BALB/c mice. Adding anti-PD1 antibodies (CpG+αOX40+αPD1) to in situ vaccinations boosts the antitumor effect. When used instead of antibodies, aptamers also possess antitumor activity, although this effect was less pronounced. The strongest effect across all the tumors was observed in highly immunogenic A20 B cell lymphoma and Erlich carcinoma.

AB - To overcome immune tolerance to cancer, the immune system needs to be exposed to a multi-target action intervention. Here, we investigated the activating effect of CpG oligodeoxynucleotides, mesyl phosphoramidate CpG oligodeoxynucleotides, anti-OX40 antibodies, and OX40 RNA aptamers on major populations of immunocompetent cells ex vivo. Comparative analysis of the antitumor effects of in situ vaccination with CpG oligodeoxynucleotides and anti-OX40 antibodies, as well as several other combinations such as mesyl phosphoramidate CpG oligodeoxynucleotides and OX40 RNA aptamers, were conducted. Antibodies against programmed death 1 (PD1) checkpoint inhibitors or corresponding PD1 DNA aptamers were also added to vaccination regimens for analytical purposes. Four scenarios were considered: a weakly immunogenic Krebs-2 carcinoma grafted in CBA mice; a moderately immunogenic Lewis carcinoma grafted in C57Black mice; and an immunogenic A20 B cell lymphoma or an Erlich carcinoma, grafted in BALB/c mice. Adding anti-PD1 antibodies (CpG+αOX40+αPD1) to in situ vaccinations boosts the antitumor effect. When used instead of antibodies, aptamers also possess antitumor activity, although this effect was less pronounced. The strongest effect across all the tumors was observed in highly immunogenic A20 B cell lymphoma and Erlich carcinoma.

KW - immunogenicity

KW - Krebs-2 carcinoma

KW - Lewis carcinoma

KW - Erlich carcinoma

KW - A20 B cell lymphoma

KW - mesyl phosphoramidate

UR - https://www.scopus.com/record/display.uri?eid=2-s2.0-85167899121&origin=inward&txGid=fda2c4d84f501b2e29f081bf42056e80

UR - https://www.mendeley.com/catalogue/2cbe445d-45f5-3964-b6d7-14c9ad824468/

U2 - 10.7555/JBR.36.20220052

DO - 10.7555/JBR.36.20220052

M3 - Article

C2 - 37161885

VL - 37

SP - 194

EP - 212

JO - Journal of Biomedical Research

JF - Journal of Biomedical Research

SN - 1674-8301

IS - 3

ER -

ID: 43869033