Antitumor Effects of Human Induced PluripotentS tem Cell-Based Cancer Vaccine on Animal Model of Breas tCancer

سال انتشار: 1401
نوع سند: مقاله کنفرانسی
زبان: انگلیسی
مشاهده: 108

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شناسه ملی سند علمی:

RROYAN23_236

تاریخ نمایه سازی: 17 دی 1401

چکیده مقاله:

Objective: S tudies on cancer as the second leading cause ofdeath, have been indicated the similarity between pluripotents tem cells (PSCs) and cancer cells in cellular and molecularcharacteris tics. This similarity has led to the hypothesis thatPSCs could be used as tumor antigens and opened new approachesfor the possibility of using PSCs for cancer treatment.Materials and Methods: The human induced pluripotent s temcell line (CAG-hiPSC) was provided from Royan S tem CellBank and cultured. The cells were prepared in lysate form beforevaccination. Cell lysate was prepared after five cycles offreeze-thawing. BALB/C mice were immunized in differentgroups with ۱) hiPSC lysate, ۲) hiPSC lysate+Adj, and ۳) Freundadjuvant (control). After three once-weekly vaccinations,۴T۱ breas t cancer cell line was injected into the mice. Immunologicalanalyzes were performed to inves tigate the immuneresponse in different treatment groups.Results: Immunohis tochemis try (IHC) s taining revealed thatthe expression of CD۸ and CD۴ markers were significantlyhigher in the tumor of hiPSC+Adj-treated mice in comparison tothe Adj-treated mice. Moreover, mice treated with hiPSC+Adjexhibited significantly increased secretion of IFN-γ and IL-۴ incomparison to the Adj-treated mice. There were no significantdifferences in the frequency of IL-۱۰ between hiPSC+Adj andAdj groups.Conclusion: Our findings sugges ted that among all the treatmentstes ted, the combination of hiPSC with Adj could providemore effective immunity in the breas t cancer mouse model byinducing anti-tumor responses

کلیدواژه ها:

Antitumor Immunity ، Cancer Vaccine ، Human PluripotentS tem Cells

نویسندگان

MS Badri

Department of Developmental Biology, Faculty of Sciensec andAdvanced Technologies in Biology, University of Science and Culture,Tehran, Iran . Department of S tem Cells and Developmental Biology, Cell ScienceResearch Center, Royan Ins titute for S tem Cel

M Zarghami

Department of Developmental Biology, Faculty of Sciensec andAdvanced Technologies in Biology, University of Science and Culture,Tehran, Iran . Department of S tem Cells and Developmental Biology, Cell ScienceResearch Center, Royan Ins titute for S tem Cel

M SABER

Department of S tem Cells and Developmental Biology, Cell ScienceResearch Center, Royan Ins titute for S tem Cell Biology andTechnology, ACECR, Tehran, Iran

F Shekari

Department of S tem Cells and Developmental Biology, Cell ScienceResearch Center, Royan Ins titute for S tem Cell Biology andTechnology, ACECR, Tehran, Iran

M Ebrahimi

Department of S tem Cells and Developmental Biology, Cell ScienceResearch Center, Royan Ins titute for S tem Cell Biology andTechnology, ACECR, Tehran, Iran

N Hassani

Department of S tem Cells and Developmental Biology, Cell ScienceResearch Center, Royan Ins titute for S tem Cell Biology andTechnology, ACECR, Tehran, Iran