By Frederick W. Alt
Advances in Immunology, a customary and hugely revered e-book, offers present advancements in addition to accomplished experiences in immunology. Articles deal with the big variety of subject matters that contain immunology, together with molecular and mobile activation mechanisms, phylogeny and molecular evolution, and medical modalities. Edited and authored by means of the key scientists within the box, every one quantity presents up to date info and instructions for the future.
- Contributions from prime authorities
- Informs and updates on all of the most modern advancements within the field
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Extra info for Advances in Immunology
2012). TGF-beta promotes proliferation of thyroid epithelial cells in IFN-gamma(-/-) mice by down-regulation of p21 and p27 via AKT pathway. The American Journal of Pathology, 180, 650–660. Good-Jacobson, K. , Szumilas, C. , Sharpe, A. , Tomayko, M. , & Shlomchik, M. J. (2010). PD-1 regulates germinal center B cell survival and the formation and affinity of long-lived plasma cells. Nature Immunology, 11, 535–542. Hamel, K. , Kehry, M. , et al. (2011). B cell depletion enhances T regulatory cell activity essential in the suppression of arthritis.
32 Helen Braley-Mullen and Shiguang Yu hypothesized that expression of CD40 on thyrocytes was a necessary step in development of TEC H/P; if so, TEC H/P should not develop in mice lacking CD40 on thyrocytes. CD40À/ÀCD28+IFN-γÀ/À mice are completely resistant to TEC H/P (Table 4; unpublished results). However, when we generated CD40À/ÀCD28À/ÀIFN-γ À/À mice to provide a more stringent test of our hypothesis, a high percentage of CD40À/À CD28À/À mice develop severe TEC H/P with fibrosis and low serum T4 8 weeks after administration of NaI in their drinking water (Table 4).
H-2h4 mice can be activated in vitro with MTg in the presence of particular cytokines such as IL-12, to transfer severe EAT to sublethally irradiated recipients (H. Braley-Mullen, unpublished results; Wei, Chen, Sharp, & Braley-Mullen, 2003). H2h4 mice can therefore be useful for EAT experiments. H-2h4 mice have shown. H-2h4 mice are resistant to EAT (H. Braley-Mullen, unpublished results). H-2h4 mice for EAT experiments. H-2h4 mice are resistant to EAT and they do not produce MTg autoantibodies following immunization.