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Immunotoxicology Strategies for Pharmaceutical Safety Assessment
Danuta J. Herzyk (Edited by), DJ Herzyk (Author), Jeanine L. Bussiere (Edited by)
9780470122389, Wiley
Hardback, published 12 September 2008
444 pages
24.4 x 16.4 x 2.6 cm, 0.748 kg
"I would recommend this book to toxicologists wishing to develop their knowledge in the specialised field of immunotoxicology. The book provides extremely clear indication on the assessment of immunotoxicology and contains many recent references at the end of each chapter." (BTS Newsletter, Summer 2009)
Preface ix Contributors xi Introduction to Immunotoxicology xvii Part I Current Regulatory Expectations For Immunotoxicity Evaluation Of Pharmaceuticals 1 1 Current Regulatory Expectations for Immunotoxicity Evaluation of Pharmaceuticals 3 Part II Weight of Evidence Review: A New Strategy In Immunotoxicology 11 2.1 Clinical Pathology as Crucial Insight into Immunotoxicity Testing 13 2.2 Histomorphology of the Immune System: A Basic Step in Assessing Immunotoxicity 27 2.3 Need for Specialized Immunotoxicity Tests 45 2.4 Specific Drug-Induced Immunotoxicity: Immune-Mediated Hemolytic Anemia 55 Part III Nonclinical Core Immunotoxicity Testing In Drug Development 65 3.1.1 T Cell-Dependent Antibody Response Tests 67 3.1.2 Natural Killer Cell Assay and Other Innate Immunity Tests 77 3.1.3 Cellular Immune Response in Delayed-Type Hypersensitivity Test 87 3.2 Evaluation of Drug Effects on Immune Cell Phenotypes 103 Part IV Extended Immunotoxicology Assessment: Ex Vivo Models 125 4.1 Functional Cellular Responses and Cytokine Profiles 127 4.2 Application of Flow Cytometry in Drug Development 141 Part V Extended Immunotoxicology Assessment: In Vivo Models 161 5.1 Animal Models of Host Resistance 163 5.2 Approaches to Evaluation of Autoimmunity 179 Part VI Immunotoxicity Testing In Biopharmaceutical Development 189 6.1 Differentiation between Desired Immunomodulation and Potential Immunotoxicity 191 6.2 Relevant Immune Tests across Different Species and Surrogate Models 199 6.3 Antidrug Antibody Responses in Nonclinical Studies and Their Implications 209 Part VII Development of Vaccines 217 7.1 Pharmacological Immunogenicity and Adverse Responses to Vaccines 219 7.2 Immunotoxicological Concerns for Vaccines and Adjuvants 229 Part VIII Testing For Drug Hypersensitivity 239 8.1 Systemic Hypersensitivity 241 8.2 Nonclinical Models to Assess Respiratory Hypersensitivity Potential 257 Part IX Testing For Developmental Immunotoxicity 271 9.1 Developmental Immunotoxicity in Rodents 273 9.2 Developmental Immunotoxicity in Nonhuman Primates 299 Part X New Methods In Assessing Immunomodulation, Immunotoxicity, and Immunogenicity 319 10.1 Alternative Animal Models for Immunomodulation and Immunotoxicity 321 10.2 Animal Models for Preclinical Comparative Immunogenicity Testing 345 10.3 T Cell Epitopes and Minimization of Immunogenicity 361 Part XI Bridging Immunotoxicology To Clinical Drug Development 373 Index 385
Jack H. Dean
Kenneth L. Hastings
Ellen Evans
Patrick Haley
Kazuichi Nakamura
Raj Krishnaraj
Joseph R. Piccotti
Lisa Plitnick
Karen Price
Laurie Iciek
Elizabeth R. Gore
Padma Narayanan, Renold J. Capocasale, Nianyu Li, and Peter J. Bugelski
Gary R. Burleson and Florence G. Burleson
Danuta J. Herzyk
Jeanine L. Bussiere and Barbara Mounho
Jeanine L. Bussiere
Barbara Mounho
Mary Kate Hart, Mark Bolanowski, and Robert V. House
Catherine Kaplanski, Jose Lebron, Jayanthi Wolf, and Brian Ledwith
Raymond Pieters
Curtis C. Maier
Rodney R. Dietert and Leigh Ann Burns-Naas
Pauline L. Martin and Eberhard Buse
Peter J. Bugelski
Daniel Wierda
Harald Kropshoffer and Thomas Singer
11 Bridging Immunotoxicology to Clinical Drug Development 375
Ian Gourley and Jacques Descotes
Subject Areas: Chemistry [PN]
