摘要 | 第1-10页 |
ABSTRACT | 第10-21页 |
PART Ⅰ.REGULATION OF B CELLS BY E2/MSC | 第21-83页 |
CHAPTER 1 THE IMMUNE REGULATION OF B CELLS BY E2 AND MSCS | 第21-38页 |
1. B CELLS BACKGROUNDS | 第21-26页 |
·B cells activation and functions | 第21-22页 |
·TLRs on B cells and TLR9 | 第22-24页 |
·B cells and autoimmune diseases | 第24-25页 |
·Charactors of human B cell lines | 第25-26页 |
2. ESTROGEN AND ROLES ON AUTOIMMUNE REGULATION | 第26-27页 |
3. THE ROLE OF MSC ON IMMUNE REGULATION | 第27-31页 |
·The background of mesenchymal stem cell | 第27-28页 |
·MSC and the therapy for autoimmune diseases | 第28-29页 |
·The modulation of MSC on immune cells | 第29-31页 |
4. REFERENCE | 第31-38页 |
CHAPTER 2 17B-ESTRADIOL ENHANCES RESPONSE OF MICE SPLEEN B CELLS ELICITED BY TLR9 AGONIST | 第38-62页 |
1. INTRODUCTION | 第38-39页 |
2. MATERIALS AND METHODS | 第39-44页 |
·Mice | 第39-40页 |
·Reagents | 第40页 |
·Isolation of B cells and cell culture | 第40-41页 |
·Viability test | 第41页 |
·B lymphocyte proliferation assay | 第41-42页 |
·Cell death assay and cell counting | 第42页 |
·Flow cytometry | 第42-43页 |
·ELISA | 第43页 |
·Microarray assay | 第43页 |
·Ovariectomy and E2 exposure | 第43-44页 |
·Statistical analysis | 第44页 |
3. RESULTS | 第44-55页 |
·E2 changed the morphology and density of B cells in vitro with CpG ODN stimulation | 第44-45页 |
·E2 improved the viability of B cells with CpG stimulation | 第45-47页 |
·E2 enhanced the expression of co-stimulatory molecules(CD86 and CD40)on B cells under the exposure to CpG ODN | 第47-48页 |
·CpG ODN induced the expression of IgM and cytokines,in which E2 enhance the IgM level in supernatant | 第48-50页 |
·In vivo experiments | 第50-53页 |
·E2 increased the expression of TLR9 and MCM6 on B cells induced by CpG | 第53-55页 |
4. DISCUSSION | 第55-59页 |
5. REFERENCE | 第59-62页 |
CHAPTER 3 MSCS REGULATE HUMAN B CELL LINES FUNCTIONS | 第62-83页 |
1. INTRODUCTION | 第62-63页 |
2. MATERIALS AND METHODS | 第63-67页 |
·Culture of human MSCs | 第63-64页 |
·Culture of B cell lines and reagents | 第64页 |
·Cell cycle analysis | 第64-65页 |
·RT and QPCR analysis | 第65-66页 |
·Flow cytometry | 第66页 |
·Western blotting | 第66-67页 |
·Statistical analysis | 第67页 |
3. RESULTS | 第67-78页 |
·The influence of MSCs on the growth of B cell lines with or without CpG-DNA stimulation | 第67-69页 |
·Inhibition of IgM and CD86 surface expressions on B cell lines by UC-MSCs | 第69-73页 |
·Cytokines and chemokines | 第73页 |
·IL-1β primed UC-MSCs promoted chemokines expression on Daudi but not the inhibition of CD86 and IgM | 第73-76页 |
·ERK signal was involved in the effect of UC-MSCs on B cell lines | 第76-78页 |
4 DISCUSSION | 第78-81页 |
5 REFERENCE | 第81-83页 |
PART Ⅱ.IL-12 IMMUNOTHERAPY OF SCC | 第83-110页 |
CHAPTER 4 IL-12 AND CANCER IMMUNOTHERAPY | 第83-91页 |
1. CYTOKINE THERAPY FOR CANCER | 第83-84页 |
2. INSERLEUKIN-12(IL-12) | 第84-85页 |
3. ROLE OF IL-12 IN IMMUNOTHERAPY | 第85-86页 |
4. LENTIVIRAL VECTORS AND SAFETY | 第86-87页 |
5. SQUAMOUS CELL CARCINOMA(SCC)AND MURINE CANCER MODELS | 第87-88页 |
6. REFERENCES | 第88-91页 |
CHAPTER 5 LOCALIZED IL-12 DELIVERY FOR IMMUNOTHERAPY OF SCC TUMOR~* | 第91-110页 |
1. INTRODUCTION | 第91-93页 |
2. MATERIALS AND METHODS | 第93-96页 |
·Lentiviral production | 第93-94页 |
·Tumor cell lines | 第94页 |
·Transduction of tumor cells and IL-12 level detection | 第94页 |
·Tumor cell growth kinetics | 第94-95页 |
·Mice | 第95页 |
·In vivo tumor experiments | 第95页 |
·T cell depletion | 第95-96页 |
·Blood cytokine analysis | 第96页 |
·Statistical analysis | 第96页 |
3. RESULTS | 第96-103页 |
·Generation of IL-12 secreting tumor cells | 第96-98页 |
·IL-12 producing cell lines were able to inhibit tumor development | 第98-99页 |
·Both CD4+ and CD8+ cells were required to eliminate IL-12 producing tumor cells | 第99页 |
·IL-12 secreting tumor cells led to the establishment of immune memory | 第99-101页 |
·A small percentage of IL-12 producing cells were able to protect mice from tumor development | 第101-102页 |
·Cell based IL-12 therapy did not lead to elevated systemic levels of inflammatory cytokines | 第102-103页 |
4. DISCUSSION | 第103-107页 |
5. REFERENCE | 第107-110页 |
博士研究生期间发表及待发表论文列表 | 第110-111页 |
致谢 | 第111-112页 |