Transfection of B7—1 cDNA empowers antigen presentation of blood malignant cells for activation of anti—tumor T cells

Ojbective To define roles of B7-1 co-stimulation factor expressed in human malignant cell lines in mediating anti-tumor T cell immune responses.Methods Examining human leucocyte antigen(HLA)and B7 expressions on 8 human blood malignancies cell lines by flow cytometry.Transtecting B7-1 gene to B7-1 n...

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Published inChinese medical journal Vol. 116; no. 1; pp. 78 - 84
Main Author 克晓燕 贾丽萍 王晶 王德炳
Format Journal Article
LanguageEnglish
Published China Department of Hematology, Third Hospital, Peking University, Beijing 100083, China%Institute of Blood Disease Research, People's Hospital, Peking University, Beijing 100083, China 2003
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ISSN0366-6999
2542-5641

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Abstract Ojbective To define roles of B7-1 co-stimulation factor expressed in human malignant cell lines in mediating anti-tumor T cell immune responses.Methods Examining human leucocyte antigen(HLA)and B7 expressions on 8 human blood malignancies cell lines by flow cytometry.Transtecting B7-1 gene to B7-1 negative(B7^-)Raji and B7^- Jurkat cell lines by liposome,and comparing the potencies of blood malignant cell lines in the induction of T cell activation by examination of T cell cytokine mRNAs before and after transtection using semi-quantitative reverse transcription polymerase chain reaction(RT-PCR). Results High level of HLA Ⅰ and Ⅱ molecules were expressed in most human blood malignant cell lines examined,and the co-stimulatory factor B7-2 was also highly expressed.In contrast,another member of B7 family:B7-1 was either not axpressed or very limitedly expressed in most of these hematopoietic malignant cell lines.Most importantly,transfection of B7-1 gene to B7^-.Raji and B7^-.Jurkat cell lines made these cell lines better antigen presenting cells for stimulation of anti-tumor T cell activation,which was demonstrated by up regulation of expression of T cell cytokines IL-2,IL-4 and INF-γ mRNAs after incubation of these tumor cells with T cells for 24h.Conclusions B7 co-stimulation plays an important role in anti-tumor immunity.Transfection of B7-1 gene to the human hematopoietic malignant cell lines that are deficient in the B7-1 expression empowers their antigen presentation potengy for activation of anti-tumor T cells.Our results suggested that repairing the deficiency of B7-1 co-stimulatory pathway in tumor cells might be a novel immunotherapeutic approach for human hematopoletic malignancies.
AbstractList Ojbective To define roles of B7-1 co-stimulation factor expressed in human malignant cell lines in mediating anti-tumor T cell immune responses.Methods Examining human leucocyte antigen(HLA)and B7 expressions on 8 human blood malignancies cell lines by flow cytometry.Transtecting B7-1 gene to B7-1 negative(B7^-)Raji and B7^- Jurkat cell lines by liposome,and comparing the potencies of blood malignant cell lines in the induction of T cell activation by examination of T cell cytokine mRNAs before and after transtection using semi-quantitative reverse transcription polymerase chain reaction(RT-PCR). Results High level of HLA Ⅰ and Ⅱ molecules were expressed in most human blood malignant cell lines examined,and the co-stimulatory factor B7-2 was also highly expressed.In contrast,another member of B7 family:B7-1 was either not axpressed or very limitedly expressed in most of these hematopoietic malignant cell lines.Most importantly,transfection of B7-1 gene to B7^-.Raji and B7^-.Jurkat cell lines made these cell lines better antigen presenting cells for stimulation of anti-tumor T cell activation,which was demonstrated by up regulation of expression of T cell cytokines IL-2,IL-4 and INF-γ mRNAs after incubation of these tumor cells with T cells for 24h.Conclusions B7 co-stimulation plays an important role in anti-tumor immunity.Transfection of B7-1 gene to the human hematopoietic malignant cell lines that are deficient in the B7-1 expression empowers their antigen presentation potengy for activation of anti-tumor T cells.Our results suggested that repairing the deficiency of B7-1 co-stimulatory pathway in tumor cells might be a novel immunotherapeutic approach for human hematopoletic malignancies.
To define roles of B7-1 co-stimulation factor expressed in human malignant cell lines in mediating anti-tumor T cell immune responses. Examining human leucocyte antigen (HLA) and B7 expressions on 8 human blood malignancies cell lines by flow cytometry. Transfecting B7-1 gene to B7-1 negative (B7(-)) Raji and B7(-) Jurkat cell lines by liposome, and comparing the potencies of blood malignant cell lines in the induction of T cell activation by examination of T cell cytokine mRNAs before and after transfection using semi-quantitative reverse transcription polymerase chain reaction (RT-PCR). High level of HLA I and II molecules were expressed in most human blood malignant cell lines examined, and the co-stimulatory factor B7-2 was also highly expressed. In contrast, another member of B7 family: B7-1 was either not expressed or very limitedly expressed in most of these hematopoietic malignant cell lines. Most importantly, transfection of B7-1 gene to B7(-). Raji and B7(-). Jurkat cell lines made these cell lines better antigen presenting cells for stimulation of anti-tumor T cell activation, which was demonstrated by up regulation of expression of T cell cytokines IL-2, IL-4 and INF-gamma mRNAs after incubation of these tumor cells with T cells for 24 h. B7 co-stimulation plays an important role in anti-tumor immunity. Transfection of B7-1 gene to the human hematopoietic malignant cell lines that are deficient in the B7-1 expression empowers their antigen presentation potency for activation of anti-tumor T cells. Our results suggested that repairing the deficiency of B7-1 co-stimulatory pathway in tumor cells might be a novel immunotherapeutic approach for human hematopoietic malignancies.
To define roles of B7-1 co-stimulation factor expressed in human malignant cell lines in mediating anti-tumor T cell immune responses.OBJECTIVETo define roles of B7-1 co-stimulation factor expressed in human malignant cell lines in mediating anti-tumor T cell immune responses.Examining human leucocyte antigen (HLA) and B7 expressions on 8 human blood malignancies cell lines by flow cytometry. Transfecting B7-1 gene to B7-1 negative (B7(-)) Raji and B7(-) Jurkat cell lines by liposome, and comparing the potencies of blood malignant cell lines in the induction of T cell activation by examination of T cell cytokine mRNAs before and after transfection using semi-quantitative reverse transcription polymerase chain reaction (RT-PCR).METHODSExamining human leucocyte antigen (HLA) and B7 expressions on 8 human blood malignancies cell lines by flow cytometry. Transfecting B7-1 gene to B7-1 negative (B7(-)) Raji and B7(-) Jurkat cell lines by liposome, and comparing the potencies of blood malignant cell lines in the induction of T cell activation by examination of T cell cytokine mRNAs before and after transfection using semi-quantitative reverse transcription polymerase chain reaction (RT-PCR).High level of HLA I and II molecules were expressed in most human blood malignant cell lines examined, and the co-stimulatory factor B7-2 was also highly expressed. In contrast, another member of B7 family: B7-1 was either not expressed or very limitedly expressed in most of these hematopoietic malignant cell lines. Most importantly, transfection of B7-1 gene to B7(-). Raji and B7(-). Jurkat cell lines made these cell lines better antigen presenting cells for stimulation of anti-tumor T cell activation, which was demonstrated by up regulation of expression of T cell cytokines IL-2, IL-4 and INF-gamma mRNAs after incubation of these tumor cells with T cells for 24 h.RESULTSHigh level of HLA I and II molecules were expressed in most human blood malignant cell lines examined, and the co-stimulatory factor B7-2 was also highly expressed. In contrast, another member of B7 family: B7-1 was either not expressed or very limitedly expressed in most of these hematopoietic malignant cell lines. Most importantly, transfection of B7-1 gene to B7(-). Raji and B7(-). Jurkat cell lines made these cell lines better antigen presenting cells for stimulation of anti-tumor T cell activation, which was demonstrated by up regulation of expression of T cell cytokines IL-2, IL-4 and INF-gamma mRNAs after incubation of these tumor cells with T cells for 24 h.B7 co-stimulation plays an important role in anti-tumor immunity. Transfection of B7-1 gene to the human hematopoietic malignant cell lines that are deficient in the B7-1 expression empowers their antigen presentation potency for activation of anti-tumor T cells. Our results suggested that repairing the deficiency of B7-1 co-stimulatory pathway in tumor cells might be a novel immunotherapeutic approach for human hematopoietic malignancies.CONCLUSIONSB7 co-stimulation plays an important role in anti-tumor immunity. Transfection of B7-1 gene to the human hematopoietic malignant cell lines that are deficient in the B7-1 expression empowers their antigen presentation potency for activation of anti-tumor T cells. Our results suggested that repairing the deficiency of B7-1 co-stimulatory pathway in tumor cells might be a novel immunotherapeutic approach for human hematopoietic malignancies.
R73; Objective To define roles of B7-1 co-stimulation factor expressed in human malignant cell lines in mediating anti-tumor T cell immune responses. Methods Examining human leucocyte antigen (HLA) and B7 expressions on 8 human blood malignancies cell lines by flow cytometry. Transfecting B7-1 gene to B7-1 negative (B7*!-) Raji and B7*!- Jurkat cell lines by liposome, and comparing the potencies of blood malignant cell lines in the induction of T cell activation by examination of T cell cytokine mRNAs before and after transfection using semi-quantitative reverse transcription polymerase chain reaction (RT-PCR). Results High level of HLA Ⅰ and Ⅱ molecules were expressed in most human blood malignant cell lines examined, and the co-stimulatory factor B7-2 was also highly expressed. In contrast, another member of B7 family: B7-1 was either not expressed or very limitedly expressed in most of these hematopoietic malignant cell lines. Most importantly, transfection of B7-1 gene to B7*!-. Raji and B7*!-. Jurkat cell lines made these cell lines better antigen presenting cells for stimulation of anti-tumor T cell activation, which was demonstrated by up regulation of expression of T cell cytokines IL-2, IL-4 and INF-γ mRNAs after incubation of these tumor cells with T cells for 24 h. Conclusions B7 co-stimulation plays an important role in anti-tumor immunity. Transfection of B7-1 gene to the human hematopoietic malignant cell lines that are deficient in the B7-1 expression empowers their antigen presentation potency for activation of anti-tumor T cells. Our results suggested that repairing the deficiency of B7-1 co-stimulatory pathway in tumor cells might be a novel immunotherapeutic approach for human hematopoietic malignancies.
Author 克晓燕 贾丽萍 王晶 王德炳
AuthorAffiliation DepartmentofHematology,ThirdHospital,PekingUniversity,Beijing100083,China InstituteofBloodDiseaseResearch,People’sHospital,PekingUniversity,Beijing100083,China
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Snippet Ojbective To define roles of B7-1 co-stimulation factor expressed in human malignant cell lines in mediating anti-tumor T cell immune responses.Methods...
To define roles of B7-1 co-stimulation factor expressed in human malignant cell lines in mediating anti-tumor T cell immune responses. Examining human...
To define roles of B7-1 co-stimulation factor expressed in human malignant cell lines in mediating anti-tumor T cell immune responses.OBJECTIVETo define roles...
R73; Objective To define roles of B7-1 co-stimulation factor expressed in human malignant cell lines in mediating anti-tumor T cell immune responses. Methods...
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SubjectTerms Antigen Presentation
Antigens, CD - analysis
B7-1 Antigen - analysis
B7-1 Antigen - physiology
B7-2 Antigen
B7-1转染
cDNA
Cytokines - genetics
Flow Cytometry
Hematologic Neoplasms - immunology
HLA-DR7 Antigen - physiology
Humans
K562 Cells
Lymphocyte Activation
Membrane Glycoproteins - analysis
RNA, Messenger - analysis
T-Lymphocytes - immunology
Transfection
U937 Cells
恶性血液病细胞系
抗原提呈
抗肿瘤T-细胞
Title Transfection of B7—1 cDNA empowers antigen presentation of blood malignant cells for activation of anti—tumor T cells
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