{"title":"B Cell Defects","authors":"RALPH J. WEDGWOOD","doi":"10.1016/S0260-4639(22)00131-1","DOIUrl":"10.1016/S0260-4639(22)00131-1","url":null,"abstract":"","PeriodicalId":100282,"journal":{"name":"Clinics in Immunology and Allergy","volume":"5 2","pages":"Pages 301-324"},"PeriodicalIF":0.0,"publicationDate":"1985-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73491770","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Immunology of the Fetus and Newborn: Lymphocyte Phenotype and Function","authors":"MARJORIE WILSON","doi":"10.1016/S0260-4639(22)00129-3","DOIUrl":"10.1016/S0260-4639(22)00129-3","url":null,"abstract":"<div><p>Lymphocyte development begins early in the first trimester of gestation, and the fetus is capable of normal cytotoxic responses and some degree of T-B cooperation early in the second trimester. Neonates, however, are not fully immunocompetent at birth. They produce a restricted library of immunoglobulin isotypes and experience a ‘physiological hypogamma-globulinaemia’ for weeks or months. Premature infants are more profoundly hypogammaglobulinaemic for a longer time, and are less able to mount an appropriate response to bacterial or viral challenge, than term infants. Phenotypic analysis of lymphocyte populations from umbilical cord blood shows that lymphoid ontogeny is reflected in changing lymphoid subpopulations in peripheral blood of neonates throughout the third trimester of gestation. Immaturities exist in both B and T cell subsets in cord blood. These irregularities are most marked in early third trimester. Moreover, certain types of severe antenatal stress may alter the normal temporal sequence of acquisition of T and B lymphocyte surface antigens. The presence of T6<sup>+</sup> cells in some cords suggests the possibility that profound stress, which causes the thymus to shrink, may also cause thymocytes to be released into circulation before the normal sequence of maturation is complete. These lymphocytes may be analogous to the ‘leftward shifted’ neutrophil band forms which are released into circulation in response to bacterial infection. Finally, newborns in general, and severely stressed or very premature newborns in particular, are at increased risk from infection not only because their immune systems are inexperienced, but primarily because their circulating T and B lymphocytes are at a stage of differentiation which may not permit them to function effectively in response to antigenic challenge.</p></div>","PeriodicalId":100282,"journal":{"name":"Clinics in Immunology and Allergy","volume":"5 2","pages":"Pages 271-286"},"PeriodicalIF":0.0,"publicationDate":"1985-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76742307","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Ontogeny of T Cells","authors":"OSIAS STUTMAN","doi":"10.1016/S0260-4639(22)00126-8","DOIUrl":"10.1016/S0260-4639(22)00126-8","url":null,"abstract":"","PeriodicalId":100282,"journal":{"name":"Clinics in Immunology and Allergy","volume":"5 2","pages":"Pages 191-234"},"PeriodicalIF":0.0,"publicationDate":"1985-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"79571532","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Index","authors":"","doi":"10.1016/S0260-4639(22)00136-0","DOIUrl":"https://doi.org/10.1016/S0260-4639(22)00136-0","url":null,"abstract":"","PeriodicalId":100282,"journal":{"name":"Clinics in Immunology and Allergy","volume":"5 2","pages":"Pages 379-383"},"PeriodicalIF":0.0,"publicationDate":"1985-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0260463922001360/pdfft?md5=8bbe147e07e0b35b1feb5df9124a12d5&pid=1-s2.0-S0260463922001360-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"137055191","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Genetic Deficiencies of the Complement System","authors":"FRED S. ROSEN, CHESTER A. ALPER","doi":"10.1016/S0260-4639(22)00135-9","DOIUrl":"10.1016/S0260-4639(22)00135-9","url":null,"abstract":"<div><p>Genetic deficiencies of almost all the 20 proteins of the complement system have been described. They are all inherited as autosomal recessive phenomena with the exception of properdin (X-linkage) and CI 1NH (autosomal dominant). The deficiencies readily fall into five categories that are distinctive but not without overlap. They present with angio-oedema (CI 1NH); immune complex disease (Clq, Or, C4, C2); susceptibility to pyogens (C3, factor H, factor I) or <em>Neisseria</em> (C5, C6, C7, C8, properdin). C9-deficient individuals appear to be mostly asymptomatic. Rapid progress is being made in understanding the molecular biology of these deficient states.</p></div>","PeriodicalId":100282,"journal":{"name":"Clinics in Immunology and Allergy","volume":"5 2","pages":"Pages 371-377"},"PeriodicalIF":0.0,"publicationDate":"1985-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89052275","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Title Page","authors":"","doi":"10.1016/S0260-4639(22)00122-0","DOIUrl":"https://doi.org/10.1016/S0260-4639(22)00122-0","url":null,"abstract":"","PeriodicalId":100282,"journal":{"name":"Clinics in Immunology and Allergy","volume":"5 2","pages":"Page iii"},"PeriodicalIF":0.0,"publicationDate":"1985-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"137055187","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Ontogeny and Control of Human IgE Synthesis","authors":"MICHAEL C. YOUNG, RAIF S. GEHA","doi":"10.1016/S0260-4639(22)00133-5","DOIUrl":"10.1016/S0260-4639(22)00133-5","url":null,"abstract":"","PeriodicalId":100282,"journal":{"name":"Clinics in Immunology and Allergy","volume":"5 2","pages":"Pages 339-349"},"PeriodicalIF":0.0,"publicationDate":"1985-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80020137","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Complement Biosynthesis","authors":"HARVEY R. COLTEN","doi":"10.1016/S0260-4639(22)00130-X","DOIUrl":"10.1016/S0260-4639(22)00130-X","url":null,"abstract":"","PeriodicalId":100282,"journal":{"name":"Clinics in Immunology and Allergy","volume":"5 2","pages":"Pages 287-300"},"PeriodicalIF":0.0,"publicationDate":"1985-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"90998784","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Phagocytic Defects","authors":"JOHN R. FOREHAND, RICHARD B. JOHNSTON","doi":"10.1016/S0260-4639(22)00134-7","DOIUrl":"https://doi.org/10.1016/S0260-4639(22)00134-7","url":null,"abstract":"<div><p>Disorders of phagocyte (primarily PMN) function have been reviewed according to the processes exhibited chronologically as the cell responds to microbial invasion, namely, adherence, Chemotaxis, phagocytosis, and killing. Emphasis has been placed on those functional disorders that have at least a partial biochemical explanation and that result in increased susceptibility to infection.</p></div>","PeriodicalId":100282,"journal":{"name":"Clinics in Immunology and Allergy","volume":"5 2","pages":"Pages 351-369"},"PeriodicalIF":0.0,"publicationDate":"1985-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"137055126","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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