Carbohydrate-Based Vaccines and Immunotherapies
Herausgeber: Guo, Zhongwu; Boons, Geert-Jan
Carbohydrate-Based Vaccines and Immunotherapies
Herausgeber: Guo, Zhongwu; Boons, Geert-Jan
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Studies of vaccines derived from carbohydrate antigens have seen great progress. Synthetic carbohydrate-based vaccines, including polysaccharides, neoglycoproteins, and neoglycolipids, have been explored or used to prevent and treat bacterial and viral infections, cancer, and other diseases. This book discusses these developments with a focus on glycoimmunology including the design, synthesis, evaluation, and applications of various carbohydrate-based vaccines. It approaches vaccine design from a chemistry and molecular focus, different from past work but in-tune with current advances,…mehr
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Studies of vaccines derived from carbohydrate antigens have seen great progress. Synthetic carbohydrate-based vaccines, including polysaccharides, neoglycoproteins, and neoglycolipids, have been explored or used to prevent and treat bacterial and viral infections, cancer, and other diseases. This book discusses these developments with a focus on glycoimmunology including the design, synthesis, evaluation, and applications of various carbohydrate-based vaccines. It approaches vaccine design from a chemistry and molecular focus, different from past work but in-tune with current advances, providing a single, convenient source of state-of-the-art information from leading authorities in the field.
The fundamental science and the latest developments in carbohydrate-based vaccines The relatively new field of glycoimmunology has emerged from the marriage of glycobiology and immunology, in recognition of the important role carbohydrates play as antigenic determinants. Carbohydrate-Based Vaccines and Immunotherapies comprehensively reviews the state of this exciting field, offering a single source for both the fundamental science and the latest developments. With contributions by leading experts, this resource covers the design, synthesis, evaluation, and applications of various carbohydrate-based vaccines, including polysaccharides, neoglycoproteins, and neoglycolipids. The text approaches vaccine design from a chemical and molecular focus, staying in line with current advances. Key topics covered by Carbohydrate-Based Vaccines and Immunotherapies include: * Recent developments towards clinically useful vaccines against bacteria, viruses, parasites, and fungi * Using adjuvants to improve immunogenicity and/or immunological properties of vaccines * Choosing and designing proper adjuvants for specific targets * Abnormal carbohydrates expressed by tumors * Carbohydrate-based therapeutic cancer vaccines or cancer immunotherapy * Clinical trials results for synthetic cancer vaccines * Glycoengineering of cell surface carborhydrates and its anticancer applications * Using cell surface carbohydrates for disease diagnosis A single, convenient source of state-of-the-art information from leading authorities in the field, Carbohydrate-Based Vaccines and Immunotherapies is an essential reference for organic chemists and biochemists, academic researchers, and other students and professionals involved in vaccine design.
The fundamental science and the latest developments in carbohydrate-based vaccines The relatively new field of glycoimmunology has emerged from the marriage of glycobiology and immunology, in recognition of the important role carbohydrates play as antigenic determinants. Carbohydrate-Based Vaccines and Immunotherapies comprehensively reviews the state of this exciting field, offering a single source for both the fundamental science and the latest developments. With contributions by leading experts, this resource covers the design, synthesis, evaluation, and applications of various carbohydrate-based vaccines, including polysaccharides, neoglycoproteins, and neoglycolipids. The text approaches vaccine design from a chemical and molecular focus, staying in line with current advances. Key topics covered by Carbohydrate-Based Vaccines and Immunotherapies include: * Recent developments towards clinically useful vaccines against bacteria, viruses, parasites, and fungi * Using adjuvants to improve immunogenicity and/or immunological properties of vaccines * Choosing and designing proper adjuvants for specific targets * Abnormal carbohydrates expressed by tumors * Carbohydrate-based therapeutic cancer vaccines or cancer immunotherapy * Clinical trials results for synthetic cancer vaccines * Glycoengineering of cell surface carborhydrates and its anticancer applications * Using cell surface carbohydrates for disease diagnosis A single, convenient source of state-of-the-art information from leading authorities in the field, Carbohydrate-Based Vaccines and Immunotherapies is an essential reference for organic chemists and biochemists, academic researchers, and other students and professionals involved in vaccine design.
Produktdetails
- Produktdetails
- Verlag: John Wiley & Sons / Wiley
- Seitenzahl: 434
- Erscheinungstermin: 1. Juni 2009
- Englisch
- Abmessung: 240mm x 161mm x 28mm
- Gewicht: 818g
- ISBN-13: 9780470197561
- ISBN-10: 0470197560
- Artikelnr.: 26173481
- Verlag: John Wiley & Sons / Wiley
- Seitenzahl: 434
- Erscheinungstermin: 1. Juni 2009
- Englisch
- Abmessung: 240mm x 161mm x 28mm
- Gewicht: 818g
- ISBN-13: 9780470197561
- ISBN-10: 0470197560
- Artikelnr.: 26173481
Zhongwu Guo is a Professor of Chemistry at Wayne State University. The winner of the American Chemical Society's 2005 New Investigator Award in Carbohydrate Chemistry, Dr. Guo serves on the editorial board of the Journal of Carbohydrate Chemistry, speaks regularly at international conferences, and has authored more than ninety peer-reviewed publications. Geert-Jan Boons is a Franklin Professor of Chemistry at the Complex Carbohydrate Research Center (CRCR) of the University of Georgia. The winner of the European Carbohydrate Association's Carbohydrate Research Award for Creativity in Carbohydrate Science, and the American Chemical Society's Horace Isbell Award, Dr. Boons serves on the editorial boards of Journal of Carbohydrate Chemistry and Advances in Carbohydrate Chemistry and Biochemistry.
Preface. Contributors. Chapter 1: Glycobiology and Immunology (Udayanath
Aich and Kevin J. Yarema). 1. Introduction. 2. Glycobiology. 2.1
Glycosylation - Is it Worth the Cost. 2.2 Glycan Biosynthesis - A
Dauntingly Complex Process. 2.3 Glycoproteins. 2.4 Lipid-based Glycans. 2.5
Polysaccharides: Glycosaminoglycans (GAGs) and Bacterial Capsular
Components. 3. The Immune System. 3.1 Introductory Comments. 3.2 Overview
of the Immune System. 3.3 Glycoimmunobiology. 3.4 The Interplay between
Glycosylation and Sugars is a Two Way Street. 4. Carbohydrate Antigens. 4.1
Carbohydrate Antigens in Man. 4.2 Carbohydrates and Pathogens. 4.3
Carbohydrate-based Vaccines. 4.4 Concluding Comments: Building on Success.
Acknowledgement. References Cited. Chapter 2: Preparation of Glycoconjugate
Vaccines (Wei Zou and Harold J. Jennings). 1. Introduction. 2. Capsular
Polysaccharide-Protein Conjugates. 2.1 Haemophilus influenzae type b. 2.2
Streptococcus pneumoniae. 2.3 Neisseria meningitidis. 2.4 Salmonella typhi
Vi. 2.5 Group B streptococcus. 2.6 Staphylococcus aureus type 5 and 8. 3.
Lipopolysaccharide (LPS) and Lipooligosaccharide (LOS) conjugates. 3.1
Escherichia coli O157. 3.2 Vibrio cholerae O1 and O139. 3.3 Shigella
dysenteriae type 1, sonnei and flexneri 2a. 3.4 Neisseria meningitidis and
Non-typeable Haemophilus influenzae. 4. Total synthetic glycoconjugate
vaccines. References Cited. Chapter 3: Adjuvants for Protein- and
Carbohydrate-Based Vaccines (Bruno Guy). 1. Introduction. 2. Initiation and
stimulation of adaptive responses. 3. "Old" adjuvants and formulations.
3.1. Aluminium. 3.2. Emulsions. 3.3. Saponins, QS21, ISCOMS. 3.4.
Liposomes, microparticles. 3.5. Antigen/formulation targeting. 3.6.
Induction of CD8 CTLs with soluble antigens. 4. Renaissance of innate
immunity. 4.1. TLRs, agonists and roles. 4.2. Non-TLRs innate receptors.
4.3. Other receptors involved in antigen capture and recognition. 5. From
basic research to practical applications: identification of new adjuvants.
5.1. TLR synthetic agonists. 5.2. Combination of PRR agonists. 6. Adjuvants
for carbohydrate-based vaccines. 6.1. Td and Ti B cell responses. 6.2.
Adjuvants for "free" polysaccharides (Ti antigens). 6.3. Adjuvants for
glycoconjugate vaccines (T-dependent antigens). 7. Combinations of
adjuvants: preclinical and clinical developments. 8. Immunomodulation of
existing responses: adjuvants for therapeutic vaccines. 9. Take another
route. 9.1. Adjuvants for mucosal immunization. 9.2. Epidermal or
intradermal routes. 10. Practical aspects of adjuvant development. 10.1.
Regulatory aspects. 10.2. Safety versus efficacy: risk/benefit ratio. 11.
Preclinical models used in adjuvant development. 11.1. Animal models. 11.2.
In vitro models. 12. Conclusions and perspectives. Acknowledgement.
References Cited. Chapter 4: Carbohydrate-Based Antibacterial Vaccines
(Robert A. Pon and Harold J. Jennings). 1. Introduction. 2. Polysaccharide
and glycoconjugate immunobiology. 3. Deficiencies in the human immune
response to polysaccharides. 4. Glycoconjugate vaccines. 5. Haemophilus
influenzae. 5.1 Hib polysaccharides. 5.2 Hib conjugate vaccines. 6.
Neisseria meningitidis. 6.1 Meningococcal polysaccharide vaccines. 6.2
Meningococcal conjugate vaccines. 7. Streptococcus pneumoniae. 7.1 Impact
on invasive pneumococcal disease. 7.2 Impact on acute otitis media. 8.
Group B Streptococcus. 9. Salmonella typhi. 10. Conjugate vaccines- Future
concerns. 11. Summary. References Cited. Chapter 5: Carbohydrate-Based
Antiviral Vaccines (Benjamin M. Swarts and Zhongwu Guo). 1. Introduction.
2. Viral Glycosylation. 2.1 Viral N-glycosylation. 2.2 Carbohydrates of
HIV. 2.3 Carbohydrates of influenza A virus. 2.4 Carbohydrates in hepatits
C virus. 2.5 Carbohydrates in other viruses. 3. Vaccine and Drug
Development. 3.1 HIV. 3.2. Influenza A virus. 3.3. Hepatitis C virus. 4.
Conclusions. Acknowledgement. References Cited. Chapter 6:
Carbohydrate-Based Antiparasitic Vaccines (Faustin Kamena, Xinyu Liu and
Peter H. Seeberger). 1. Introduction. 2. GPI-based antimalarial vaccine.
2.1 GPI as a malaria toxin. 2.2 Synthetic GPI as antitoxic malaria vaccine
candidate. 2.3 Synthetic GPI microarray to define antimalarial antibody
response. 3. LPG-based antileishmanial vaccine. 3.1 LPG in leishmaniasis
pathogenesis. 3.2 Synthetic phosphoglycan repeating unit as potential
antileishmanial vaccine. 3.3 Synthetic LPG cap oligosaccharide as
antileishmanial vaccine candidate. 4. Other examples. 4.1 Fucosylated
N-glycan as potential vaccine lead against schistosomiasis. 4.2 GPIs as
potential vaccine lead against toxoplasmosis and chagas' disease. 5.
Perspectives and Future Challenge. Acknowledgement. References cited.
Chapter 7: Carbohydrate-Based Antifungal Vaccines (Magdia De Jesus,
Liise-anne Pirofski and Arturo Casadevall). 1. Introduction. 2.
Terminology. 2.1 Vaccination vs Immunization. 2.2 Toxoids. 2.3
Glycoconjugates. 3. antifungal Glycoconjugate vaccines. 3.1 C. neoformans
polysaccharide-protein conjugates. 3.2 Development of alternative vaccines
in C. neoformans. 3.3 C. albicans mannan-protein conjugates. 3.4
²-Glucan-protein conjugates. 4. Antifungal vaccines and the immune system.
5. Summary. Acknowledgement. References Cited. Chapter 8: Cancer-Associated
and Related Glycosphingolipid Antigens (Steve Levery). 1. Introduction. 2.
Structural Classification of Antigens. 3. "Abnormal" Expression of
Glycosphingolipid (GSL) Glycan Structures in Cancer Tissues. 4. Discussion
of Delected Antigens. 4.1 Globo-series and related antigens. 4.2
Ganglio-series antigens. 4.3 Lacto-series (Type 1 chain; Lcn) antigens. 4.4
Neolacto-series (Type 2 chain; nLcx) antigens. 5. Other Antigens. 5.1
Lea-Lea and Leb-Lea. 5.2 Lea-Lex. Acknowledgement. References Cited.
Chapter 9: Synthetic Carbohydrate-Based Anticancer Vaccines (Therese
Buskas, Pamela Thompson, and Geert-Jan Boons). 1. Introduction to Cancer
Vaccines. 2. Tumor-Associated Carbohydrate Antigens (TACAs). 3.
Carbohydrate-Based Cancer Vaccines. 4. Humoral Immune Response to
Carbohydrates. 5. MHC Mediated Immune Response to Glycopeptides. 6.
Toll-like Receptors and the Link Between Innate and Adaptive Immunity. 7.
Chemical synthesis of tumor-associated carbohydrates and glycopeptides. 8.
Semi-synthetic carbohydrate-based cancer vaccines. 9. Fully synthetic
carbohydrate-based cancer vaccines. 10. B-epitope and receptor ligand
di-epitope constructs. 11. B- and T-cell di-epitope constructs. 12.
Tri-component vaccines. References. Chapter 10: Glycoengineering of Cell
Surface Sialic Acid and Its Application to Cancer Immunotherapy (Zhongwu
Guo). 1. Introduction. 2. Engineering of Cell Surface Sialic Acids. 3.
Sialic Acid engineering for Modulation of Cell Surface Reactivity. 4.
Sialic Acids engineering for Cancer Immunotherapy. 5. Summary.
Acknowledgement. References Cited. Chapter 11: Therapeutic Cancer Vaccines:
Clinical Trials and Applications (Hans H. Wandall and Mads A. Tarp). 1.
Introduction. 2. Innate and adaptive immunity in relation to cancer
immunotherapy. 3. Design issues for clinical cancer vaccine trials. 4.
Clinical development of cancer vaccines. 5. Proof of principle trials. 5.1
Toxicity and pharmacokinetics. 5.2 Dose and administration schedule. 5.3
Endpoints: Biological activity and clinical activity. 6. Efficacy Trials.
7. Clinical endpoints in efficacy trials. 8. Challenges in vaccine
development. 9. Defining the target tumor-associated antigens. 10.
Production and storage issues. 11. Clinical trials. 11.1
Glycosphingolipid-based vaccines. 11.2 O-glycan-based vaccines. 12.
Conclusions. Acknowledgement. References Cited. Chapter 12: Carbohydrates
as Unique Structures for Disease Diagnosis (Kate Rittenhouse-Olson). 1.
Introduction. 2. Viruses. 2.1 Infectious mononucleosis. 2.2 Influenza A and
B. 3. Bacteria. 3.1 Streptococcus pyogenes. 3.2 Groups A, B, C, D, F and G
Streptococcus. 3.3 Streptococcus pneumoniae. 3.4 Meningitis. 3.5 Chlamydia
trachomatis. 3.6 Future. 4. Fungi. 4.1 Aspergillus fumigatus. 4.2 Invasive
Candidiasis. 4.3 Cryptococcus neoformans. 4.4 Histoplasma capsulatum. 5.
Parasites. 5.1 Echinococcus multilocularis. 5.2 Clonorchis sinensis. 5.3
Trichinella. 5.4 Schistomsoma mansoni. 6. Autoimmunity. 6.1 Diabetes. 6.2
Cold agglutinin disease. 6.3 Inflammatory bowel disease. 7. Tumors. 7.1
Bladder. 7.2 Breast. 7.3 Colon. 7.4 Liver. 7.5 Lung. 7.6 Melanoma. 7.7
Ovarian. 7.8 Pancreatic. 7.9 Prostate. 8. Inherited or acquired disorders
of glycosylation. References Cited.
Aich and Kevin J. Yarema). 1. Introduction. 2. Glycobiology. 2.1
Glycosylation - Is it Worth the Cost. 2.2 Glycan Biosynthesis - A
Dauntingly Complex Process. 2.3 Glycoproteins. 2.4 Lipid-based Glycans. 2.5
Polysaccharides: Glycosaminoglycans (GAGs) and Bacterial Capsular
Components. 3. The Immune System. 3.1 Introductory Comments. 3.2 Overview
of the Immune System. 3.3 Glycoimmunobiology. 3.4 The Interplay between
Glycosylation and Sugars is a Two Way Street. 4. Carbohydrate Antigens. 4.1
Carbohydrate Antigens in Man. 4.2 Carbohydrates and Pathogens. 4.3
Carbohydrate-based Vaccines. 4.4 Concluding Comments: Building on Success.
Acknowledgement. References Cited. Chapter 2: Preparation of Glycoconjugate
Vaccines (Wei Zou and Harold J. Jennings). 1. Introduction. 2. Capsular
Polysaccharide-Protein Conjugates. 2.1 Haemophilus influenzae type b. 2.2
Streptococcus pneumoniae. 2.3 Neisseria meningitidis. 2.4 Salmonella typhi
Vi. 2.5 Group B streptococcus. 2.6 Staphylococcus aureus type 5 and 8. 3.
Lipopolysaccharide (LPS) and Lipooligosaccharide (LOS) conjugates. 3.1
Escherichia coli O157. 3.2 Vibrio cholerae O1 and O139. 3.3 Shigella
dysenteriae type 1, sonnei and flexneri 2a. 3.4 Neisseria meningitidis and
Non-typeable Haemophilus influenzae. 4. Total synthetic glycoconjugate
vaccines. References Cited. Chapter 3: Adjuvants for Protein- and
Carbohydrate-Based Vaccines (Bruno Guy). 1. Introduction. 2. Initiation and
stimulation of adaptive responses. 3. "Old" adjuvants and formulations.
3.1. Aluminium. 3.2. Emulsions. 3.3. Saponins, QS21, ISCOMS. 3.4.
Liposomes, microparticles. 3.5. Antigen/formulation targeting. 3.6.
Induction of CD8 CTLs with soluble antigens. 4. Renaissance of innate
immunity. 4.1. TLRs, agonists and roles. 4.2. Non-TLRs innate receptors.
4.3. Other receptors involved in antigen capture and recognition. 5. From
basic research to practical applications: identification of new adjuvants.
5.1. TLR synthetic agonists. 5.2. Combination of PRR agonists. 6. Adjuvants
for carbohydrate-based vaccines. 6.1. Td and Ti B cell responses. 6.2.
Adjuvants for "free" polysaccharides (Ti antigens). 6.3. Adjuvants for
glycoconjugate vaccines (T-dependent antigens). 7. Combinations of
adjuvants: preclinical and clinical developments. 8. Immunomodulation of
existing responses: adjuvants for therapeutic vaccines. 9. Take another
route. 9.1. Adjuvants for mucosal immunization. 9.2. Epidermal or
intradermal routes. 10. Practical aspects of adjuvant development. 10.1.
Regulatory aspects. 10.2. Safety versus efficacy: risk/benefit ratio. 11.
Preclinical models used in adjuvant development. 11.1. Animal models. 11.2.
In vitro models. 12. Conclusions and perspectives. Acknowledgement.
References Cited. Chapter 4: Carbohydrate-Based Antibacterial Vaccines
(Robert A. Pon and Harold J. Jennings). 1. Introduction. 2. Polysaccharide
and glycoconjugate immunobiology. 3. Deficiencies in the human immune
response to polysaccharides. 4. Glycoconjugate vaccines. 5. Haemophilus
influenzae. 5.1 Hib polysaccharides. 5.2 Hib conjugate vaccines. 6.
Neisseria meningitidis. 6.1 Meningococcal polysaccharide vaccines. 6.2
Meningococcal conjugate vaccines. 7. Streptococcus pneumoniae. 7.1 Impact
on invasive pneumococcal disease. 7.2 Impact on acute otitis media. 8.
Group B Streptococcus. 9. Salmonella typhi. 10. Conjugate vaccines- Future
concerns. 11. Summary. References Cited. Chapter 5: Carbohydrate-Based
Antiviral Vaccines (Benjamin M. Swarts and Zhongwu Guo). 1. Introduction.
2. Viral Glycosylation. 2.1 Viral N-glycosylation. 2.2 Carbohydrates of
HIV. 2.3 Carbohydrates of influenza A virus. 2.4 Carbohydrates in hepatits
C virus. 2.5 Carbohydrates in other viruses. 3. Vaccine and Drug
Development. 3.1 HIV. 3.2. Influenza A virus. 3.3. Hepatitis C virus. 4.
Conclusions. Acknowledgement. References Cited. Chapter 6:
Carbohydrate-Based Antiparasitic Vaccines (Faustin Kamena, Xinyu Liu and
Peter H. Seeberger). 1. Introduction. 2. GPI-based antimalarial vaccine.
2.1 GPI as a malaria toxin. 2.2 Synthetic GPI as antitoxic malaria vaccine
candidate. 2.3 Synthetic GPI microarray to define antimalarial antibody
response. 3. LPG-based antileishmanial vaccine. 3.1 LPG in leishmaniasis
pathogenesis. 3.2 Synthetic phosphoglycan repeating unit as potential
antileishmanial vaccine. 3.3 Synthetic LPG cap oligosaccharide as
antileishmanial vaccine candidate. 4. Other examples. 4.1 Fucosylated
N-glycan as potential vaccine lead against schistosomiasis. 4.2 GPIs as
potential vaccine lead against toxoplasmosis and chagas' disease. 5.
Perspectives and Future Challenge. Acknowledgement. References cited.
Chapter 7: Carbohydrate-Based Antifungal Vaccines (Magdia De Jesus,
Liise-anne Pirofski and Arturo Casadevall). 1. Introduction. 2.
Terminology. 2.1 Vaccination vs Immunization. 2.2 Toxoids. 2.3
Glycoconjugates. 3. antifungal Glycoconjugate vaccines. 3.1 C. neoformans
polysaccharide-protein conjugates. 3.2 Development of alternative vaccines
in C. neoformans. 3.3 C. albicans mannan-protein conjugates. 3.4
²-Glucan-protein conjugates. 4. Antifungal vaccines and the immune system.
5. Summary. Acknowledgement. References Cited. Chapter 8: Cancer-Associated
and Related Glycosphingolipid Antigens (Steve Levery). 1. Introduction. 2.
Structural Classification of Antigens. 3. "Abnormal" Expression of
Glycosphingolipid (GSL) Glycan Structures in Cancer Tissues. 4. Discussion
of Delected Antigens. 4.1 Globo-series and related antigens. 4.2
Ganglio-series antigens. 4.3 Lacto-series (Type 1 chain; Lcn) antigens. 4.4
Neolacto-series (Type 2 chain; nLcx) antigens. 5. Other Antigens. 5.1
Lea-Lea and Leb-Lea. 5.2 Lea-Lex. Acknowledgement. References Cited.
Chapter 9: Synthetic Carbohydrate-Based Anticancer Vaccines (Therese
Buskas, Pamela Thompson, and Geert-Jan Boons). 1. Introduction to Cancer
Vaccines. 2. Tumor-Associated Carbohydrate Antigens (TACAs). 3.
Carbohydrate-Based Cancer Vaccines. 4. Humoral Immune Response to
Carbohydrates. 5. MHC Mediated Immune Response to Glycopeptides. 6.
Toll-like Receptors and the Link Between Innate and Adaptive Immunity. 7.
Chemical synthesis of tumor-associated carbohydrates and glycopeptides. 8.
Semi-synthetic carbohydrate-based cancer vaccines. 9. Fully synthetic
carbohydrate-based cancer vaccines. 10. B-epitope and receptor ligand
di-epitope constructs. 11. B- and T-cell di-epitope constructs. 12.
Tri-component vaccines. References. Chapter 10: Glycoengineering of Cell
Surface Sialic Acid and Its Application to Cancer Immunotherapy (Zhongwu
Guo). 1. Introduction. 2. Engineering of Cell Surface Sialic Acids. 3.
Sialic Acid engineering for Modulation of Cell Surface Reactivity. 4.
Sialic Acids engineering for Cancer Immunotherapy. 5. Summary.
Acknowledgement. References Cited. Chapter 11: Therapeutic Cancer Vaccines:
Clinical Trials and Applications (Hans H. Wandall and Mads A. Tarp). 1.
Introduction. 2. Innate and adaptive immunity in relation to cancer
immunotherapy. 3. Design issues for clinical cancer vaccine trials. 4.
Clinical development of cancer vaccines. 5. Proof of principle trials. 5.1
Toxicity and pharmacokinetics. 5.2 Dose and administration schedule. 5.3
Endpoints: Biological activity and clinical activity. 6. Efficacy Trials.
7. Clinical endpoints in efficacy trials. 8. Challenges in vaccine
development. 9. Defining the target tumor-associated antigens. 10.
Production and storage issues. 11. Clinical trials. 11.1
Glycosphingolipid-based vaccines. 11.2 O-glycan-based vaccines. 12.
Conclusions. Acknowledgement. References Cited. Chapter 12: Carbohydrates
as Unique Structures for Disease Diagnosis (Kate Rittenhouse-Olson). 1.
Introduction. 2. Viruses. 2.1 Infectious mononucleosis. 2.2 Influenza A and
B. 3. Bacteria. 3.1 Streptococcus pyogenes. 3.2 Groups A, B, C, D, F and G
Streptococcus. 3.3 Streptococcus pneumoniae. 3.4 Meningitis. 3.5 Chlamydia
trachomatis. 3.6 Future. 4. Fungi. 4.1 Aspergillus fumigatus. 4.2 Invasive
Candidiasis. 4.3 Cryptococcus neoformans. 4.4 Histoplasma capsulatum. 5.
Parasites. 5.1 Echinococcus multilocularis. 5.2 Clonorchis sinensis. 5.3
Trichinella. 5.4 Schistomsoma mansoni. 6. Autoimmunity. 6.1 Diabetes. 6.2
Cold agglutinin disease. 6.3 Inflammatory bowel disease. 7. Tumors. 7.1
Bladder. 7.2 Breast. 7.3 Colon. 7.4 Liver. 7.5 Lung. 7.6 Melanoma. 7.7
Ovarian. 7.8 Pancreatic. 7.9 Prostate. 8. Inherited or acquired disorders
of glycosylation. References Cited.
Preface. Contributors. Chapter 1: Glycobiology and Immunology (Udayanath
Aich and Kevin J. Yarema). 1. Introduction. 2. Glycobiology. 2.1
Glycosylation - Is it Worth the Cost. 2.2 Glycan Biosynthesis - A
Dauntingly Complex Process. 2.3 Glycoproteins. 2.4 Lipid-based Glycans. 2.5
Polysaccharides: Glycosaminoglycans (GAGs) and Bacterial Capsular
Components. 3. The Immune System. 3.1 Introductory Comments. 3.2 Overview
of the Immune System. 3.3 Glycoimmunobiology. 3.4 The Interplay between
Glycosylation and Sugars is a Two Way Street. 4. Carbohydrate Antigens. 4.1
Carbohydrate Antigens in Man. 4.2 Carbohydrates and Pathogens. 4.3
Carbohydrate-based Vaccines. 4.4 Concluding Comments: Building on Success.
Acknowledgement. References Cited. Chapter 2: Preparation of Glycoconjugate
Vaccines (Wei Zou and Harold J. Jennings). 1. Introduction. 2. Capsular
Polysaccharide-Protein Conjugates. 2.1 Haemophilus influenzae type b. 2.2
Streptococcus pneumoniae. 2.3 Neisseria meningitidis. 2.4 Salmonella typhi
Vi. 2.5 Group B streptococcus. 2.6 Staphylococcus aureus type 5 and 8. 3.
Lipopolysaccharide (LPS) and Lipooligosaccharide (LOS) conjugates. 3.1
Escherichia coli O157. 3.2 Vibrio cholerae O1 and O139. 3.3 Shigella
dysenteriae type 1, sonnei and flexneri 2a. 3.4 Neisseria meningitidis and
Non-typeable Haemophilus influenzae. 4. Total synthetic glycoconjugate
vaccines. References Cited. Chapter 3: Adjuvants for Protein- and
Carbohydrate-Based Vaccines (Bruno Guy). 1. Introduction. 2. Initiation and
stimulation of adaptive responses. 3. "Old" adjuvants and formulations.
3.1. Aluminium. 3.2. Emulsions. 3.3. Saponins, QS21, ISCOMS. 3.4.
Liposomes, microparticles. 3.5. Antigen/formulation targeting. 3.6.
Induction of CD8 CTLs with soluble antigens. 4. Renaissance of innate
immunity. 4.1. TLRs, agonists and roles. 4.2. Non-TLRs innate receptors.
4.3. Other receptors involved in antigen capture and recognition. 5. From
basic research to practical applications: identification of new adjuvants.
5.1. TLR synthetic agonists. 5.2. Combination of PRR agonists. 6. Adjuvants
for carbohydrate-based vaccines. 6.1. Td and Ti B cell responses. 6.2.
Adjuvants for "free" polysaccharides (Ti antigens). 6.3. Adjuvants for
glycoconjugate vaccines (T-dependent antigens). 7. Combinations of
adjuvants: preclinical and clinical developments. 8. Immunomodulation of
existing responses: adjuvants for therapeutic vaccines. 9. Take another
route. 9.1. Adjuvants for mucosal immunization. 9.2. Epidermal or
intradermal routes. 10. Practical aspects of adjuvant development. 10.1.
Regulatory aspects. 10.2. Safety versus efficacy: risk/benefit ratio. 11.
Preclinical models used in adjuvant development. 11.1. Animal models. 11.2.
In vitro models. 12. Conclusions and perspectives. Acknowledgement.
References Cited. Chapter 4: Carbohydrate-Based Antibacterial Vaccines
(Robert A. Pon and Harold J. Jennings). 1. Introduction. 2. Polysaccharide
and glycoconjugate immunobiology. 3. Deficiencies in the human immune
response to polysaccharides. 4. Glycoconjugate vaccines. 5. Haemophilus
influenzae. 5.1 Hib polysaccharides. 5.2 Hib conjugate vaccines. 6.
Neisseria meningitidis. 6.1 Meningococcal polysaccharide vaccines. 6.2
Meningococcal conjugate vaccines. 7. Streptococcus pneumoniae. 7.1 Impact
on invasive pneumococcal disease. 7.2 Impact on acute otitis media. 8.
Group B Streptococcus. 9. Salmonella typhi. 10. Conjugate vaccines- Future
concerns. 11. Summary. References Cited. Chapter 5: Carbohydrate-Based
Antiviral Vaccines (Benjamin M. Swarts and Zhongwu Guo). 1. Introduction.
2. Viral Glycosylation. 2.1 Viral N-glycosylation. 2.2 Carbohydrates of
HIV. 2.3 Carbohydrates of influenza A virus. 2.4 Carbohydrates in hepatits
C virus. 2.5 Carbohydrates in other viruses. 3. Vaccine and Drug
Development. 3.1 HIV. 3.2. Influenza A virus. 3.3. Hepatitis C virus. 4.
Conclusions. Acknowledgement. References Cited. Chapter 6:
Carbohydrate-Based Antiparasitic Vaccines (Faustin Kamena, Xinyu Liu and
Peter H. Seeberger). 1. Introduction. 2. GPI-based antimalarial vaccine.
2.1 GPI as a malaria toxin. 2.2 Synthetic GPI as antitoxic malaria vaccine
candidate. 2.3 Synthetic GPI microarray to define antimalarial antibody
response. 3. LPG-based antileishmanial vaccine. 3.1 LPG in leishmaniasis
pathogenesis. 3.2 Synthetic phosphoglycan repeating unit as potential
antileishmanial vaccine. 3.3 Synthetic LPG cap oligosaccharide as
antileishmanial vaccine candidate. 4. Other examples. 4.1 Fucosylated
N-glycan as potential vaccine lead against schistosomiasis. 4.2 GPIs as
potential vaccine lead against toxoplasmosis and chagas' disease. 5.
Perspectives and Future Challenge. Acknowledgement. References cited.
Chapter 7: Carbohydrate-Based Antifungal Vaccines (Magdia De Jesus,
Liise-anne Pirofski and Arturo Casadevall). 1. Introduction. 2.
Terminology. 2.1 Vaccination vs Immunization. 2.2 Toxoids. 2.3
Glycoconjugates. 3. antifungal Glycoconjugate vaccines. 3.1 C. neoformans
polysaccharide-protein conjugates. 3.2 Development of alternative vaccines
in C. neoformans. 3.3 C. albicans mannan-protein conjugates. 3.4
²-Glucan-protein conjugates. 4. Antifungal vaccines and the immune system.
5. Summary. Acknowledgement. References Cited. Chapter 8: Cancer-Associated
and Related Glycosphingolipid Antigens (Steve Levery). 1. Introduction. 2.
Structural Classification of Antigens. 3. "Abnormal" Expression of
Glycosphingolipid (GSL) Glycan Structures in Cancer Tissues. 4. Discussion
of Delected Antigens. 4.1 Globo-series and related antigens. 4.2
Ganglio-series antigens. 4.3 Lacto-series (Type 1 chain; Lcn) antigens. 4.4
Neolacto-series (Type 2 chain; nLcx) antigens. 5. Other Antigens. 5.1
Lea-Lea and Leb-Lea. 5.2 Lea-Lex. Acknowledgement. References Cited.
Chapter 9: Synthetic Carbohydrate-Based Anticancer Vaccines (Therese
Buskas, Pamela Thompson, and Geert-Jan Boons). 1. Introduction to Cancer
Vaccines. 2. Tumor-Associated Carbohydrate Antigens (TACAs). 3.
Carbohydrate-Based Cancer Vaccines. 4. Humoral Immune Response to
Carbohydrates. 5. MHC Mediated Immune Response to Glycopeptides. 6.
Toll-like Receptors and the Link Between Innate and Adaptive Immunity. 7.
Chemical synthesis of tumor-associated carbohydrates and glycopeptides. 8.
Semi-synthetic carbohydrate-based cancer vaccines. 9. Fully synthetic
carbohydrate-based cancer vaccines. 10. B-epitope and receptor ligand
di-epitope constructs. 11. B- and T-cell di-epitope constructs. 12.
Tri-component vaccines. References. Chapter 10: Glycoengineering of Cell
Surface Sialic Acid and Its Application to Cancer Immunotherapy (Zhongwu
Guo). 1. Introduction. 2. Engineering of Cell Surface Sialic Acids. 3.
Sialic Acid engineering for Modulation of Cell Surface Reactivity. 4.
Sialic Acids engineering for Cancer Immunotherapy. 5. Summary.
Acknowledgement. References Cited. Chapter 11: Therapeutic Cancer Vaccines:
Clinical Trials and Applications (Hans H. Wandall and Mads A. Tarp). 1.
Introduction. 2. Innate and adaptive immunity in relation to cancer
immunotherapy. 3. Design issues for clinical cancer vaccine trials. 4.
Clinical development of cancer vaccines. 5. Proof of principle trials. 5.1
Toxicity and pharmacokinetics. 5.2 Dose and administration schedule. 5.3
Endpoints: Biological activity and clinical activity. 6. Efficacy Trials.
7. Clinical endpoints in efficacy trials. 8. Challenges in vaccine
development. 9. Defining the target tumor-associated antigens. 10.
Production and storage issues. 11. Clinical trials. 11.1
Glycosphingolipid-based vaccines. 11.2 O-glycan-based vaccines. 12.
Conclusions. Acknowledgement. References Cited. Chapter 12: Carbohydrates
as Unique Structures for Disease Diagnosis (Kate Rittenhouse-Olson). 1.
Introduction. 2. Viruses. 2.1 Infectious mononucleosis. 2.2 Influenza A and
B. 3. Bacteria. 3.1 Streptococcus pyogenes. 3.2 Groups A, B, C, D, F and G
Streptococcus. 3.3 Streptococcus pneumoniae. 3.4 Meningitis. 3.5 Chlamydia
trachomatis. 3.6 Future. 4. Fungi. 4.1 Aspergillus fumigatus. 4.2 Invasive
Candidiasis. 4.3 Cryptococcus neoformans. 4.4 Histoplasma capsulatum. 5.
Parasites. 5.1 Echinococcus multilocularis. 5.2 Clonorchis sinensis. 5.3
Trichinella. 5.4 Schistomsoma mansoni. 6. Autoimmunity. 6.1 Diabetes. 6.2
Cold agglutinin disease. 6.3 Inflammatory bowel disease. 7. Tumors. 7.1
Bladder. 7.2 Breast. 7.3 Colon. 7.4 Liver. 7.5 Lung. 7.6 Melanoma. 7.7
Ovarian. 7.8 Pancreatic. 7.9 Prostate. 8. Inherited or acquired disorders
of glycosylation. References Cited.
Aich and Kevin J. Yarema). 1. Introduction. 2. Glycobiology. 2.1
Glycosylation - Is it Worth the Cost. 2.2 Glycan Biosynthesis - A
Dauntingly Complex Process. 2.3 Glycoproteins. 2.4 Lipid-based Glycans. 2.5
Polysaccharides: Glycosaminoglycans (GAGs) and Bacterial Capsular
Components. 3. The Immune System. 3.1 Introductory Comments. 3.2 Overview
of the Immune System. 3.3 Glycoimmunobiology. 3.4 The Interplay between
Glycosylation and Sugars is a Two Way Street. 4. Carbohydrate Antigens. 4.1
Carbohydrate Antigens in Man. 4.2 Carbohydrates and Pathogens. 4.3
Carbohydrate-based Vaccines. 4.4 Concluding Comments: Building on Success.
Acknowledgement. References Cited. Chapter 2: Preparation of Glycoconjugate
Vaccines (Wei Zou and Harold J. Jennings). 1. Introduction. 2. Capsular
Polysaccharide-Protein Conjugates. 2.1 Haemophilus influenzae type b. 2.2
Streptococcus pneumoniae. 2.3 Neisseria meningitidis. 2.4 Salmonella typhi
Vi. 2.5 Group B streptococcus. 2.6 Staphylococcus aureus type 5 and 8. 3.
Lipopolysaccharide (LPS) and Lipooligosaccharide (LOS) conjugates. 3.1
Escherichia coli O157. 3.2 Vibrio cholerae O1 and O139. 3.3 Shigella
dysenteriae type 1, sonnei and flexneri 2a. 3.4 Neisseria meningitidis and
Non-typeable Haemophilus influenzae. 4. Total synthetic glycoconjugate
vaccines. References Cited. Chapter 3: Adjuvants for Protein- and
Carbohydrate-Based Vaccines (Bruno Guy). 1. Introduction. 2. Initiation and
stimulation of adaptive responses. 3. "Old" adjuvants and formulations.
3.1. Aluminium. 3.2. Emulsions. 3.3. Saponins, QS21, ISCOMS. 3.4.
Liposomes, microparticles. 3.5. Antigen/formulation targeting. 3.6.
Induction of CD8 CTLs with soluble antigens. 4. Renaissance of innate
immunity. 4.1. TLRs, agonists and roles. 4.2. Non-TLRs innate receptors.
4.3. Other receptors involved in antigen capture and recognition. 5. From
basic research to practical applications: identification of new adjuvants.
5.1. TLR synthetic agonists. 5.2. Combination of PRR agonists. 6. Adjuvants
for carbohydrate-based vaccines. 6.1. Td and Ti B cell responses. 6.2.
Adjuvants for "free" polysaccharides (Ti antigens). 6.3. Adjuvants for
glycoconjugate vaccines (T-dependent antigens). 7. Combinations of
adjuvants: preclinical and clinical developments. 8. Immunomodulation of
existing responses: adjuvants for therapeutic vaccines. 9. Take another
route. 9.1. Adjuvants for mucosal immunization. 9.2. Epidermal or
intradermal routes. 10. Practical aspects of adjuvant development. 10.1.
Regulatory aspects. 10.2. Safety versus efficacy: risk/benefit ratio. 11.
Preclinical models used in adjuvant development. 11.1. Animal models. 11.2.
In vitro models. 12. Conclusions and perspectives. Acknowledgement.
References Cited. Chapter 4: Carbohydrate-Based Antibacterial Vaccines
(Robert A. Pon and Harold J. Jennings). 1. Introduction. 2. Polysaccharide
and glycoconjugate immunobiology. 3. Deficiencies in the human immune
response to polysaccharides. 4. Glycoconjugate vaccines. 5. Haemophilus
influenzae. 5.1 Hib polysaccharides. 5.2 Hib conjugate vaccines. 6.
Neisseria meningitidis. 6.1 Meningococcal polysaccharide vaccines. 6.2
Meningococcal conjugate vaccines. 7. Streptococcus pneumoniae. 7.1 Impact
on invasive pneumococcal disease. 7.2 Impact on acute otitis media. 8.
Group B Streptococcus. 9. Salmonella typhi. 10. Conjugate vaccines- Future
concerns. 11. Summary. References Cited. Chapter 5: Carbohydrate-Based
Antiviral Vaccines (Benjamin M. Swarts and Zhongwu Guo). 1. Introduction.
2. Viral Glycosylation. 2.1 Viral N-glycosylation. 2.2 Carbohydrates of
HIV. 2.3 Carbohydrates of influenza A virus. 2.4 Carbohydrates in hepatits
C virus. 2.5 Carbohydrates in other viruses. 3. Vaccine and Drug
Development. 3.1 HIV. 3.2. Influenza A virus. 3.3. Hepatitis C virus. 4.
Conclusions. Acknowledgement. References Cited. Chapter 6:
Carbohydrate-Based Antiparasitic Vaccines (Faustin Kamena, Xinyu Liu and
Peter H. Seeberger). 1. Introduction. 2. GPI-based antimalarial vaccine.
2.1 GPI as a malaria toxin. 2.2 Synthetic GPI as antitoxic malaria vaccine
candidate. 2.3 Synthetic GPI microarray to define antimalarial antibody
response. 3. LPG-based antileishmanial vaccine. 3.1 LPG in leishmaniasis
pathogenesis. 3.2 Synthetic phosphoglycan repeating unit as potential
antileishmanial vaccine. 3.3 Synthetic LPG cap oligosaccharide as
antileishmanial vaccine candidate. 4. Other examples. 4.1 Fucosylated
N-glycan as potential vaccine lead against schistosomiasis. 4.2 GPIs as
potential vaccine lead against toxoplasmosis and chagas' disease. 5.
Perspectives and Future Challenge. Acknowledgement. References cited.
Chapter 7: Carbohydrate-Based Antifungal Vaccines (Magdia De Jesus,
Liise-anne Pirofski and Arturo Casadevall). 1. Introduction. 2.
Terminology. 2.1 Vaccination vs Immunization. 2.2 Toxoids. 2.3
Glycoconjugates. 3. antifungal Glycoconjugate vaccines. 3.1 C. neoformans
polysaccharide-protein conjugates. 3.2 Development of alternative vaccines
in C. neoformans. 3.3 C. albicans mannan-protein conjugates. 3.4
²-Glucan-protein conjugates. 4. Antifungal vaccines and the immune system.
5. Summary. Acknowledgement. References Cited. Chapter 8: Cancer-Associated
and Related Glycosphingolipid Antigens (Steve Levery). 1. Introduction. 2.
Structural Classification of Antigens. 3. "Abnormal" Expression of
Glycosphingolipid (GSL) Glycan Structures in Cancer Tissues. 4. Discussion
of Delected Antigens. 4.1 Globo-series and related antigens. 4.2
Ganglio-series antigens. 4.3 Lacto-series (Type 1 chain; Lcn) antigens. 4.4
Neolacto-series (Type 2 chain; nLcx) antigens. 5. Other Antigens. 5.1
Lea-Lea and Leb-Lea. 5.2 Lea-Lex. Acknowledgement. References Cited.
Chapter 9: Synthetic Carbohydrate-Based Anticancer Vaccines (Therese
Buskas, Pamela Thompson, and Geert-Jan Boons). 1. Introduction to Cancer
Vaccines. 2. Tumor-Associated Carbohydrate Antigens (TACAs). 3.
Carbohydrate-Based Cancer Vaccines. 4. Humoral Immune Response to
Carbohydrates. 5. MHC Mediated Immune Response to Glycopeptides. 6.
Toll-like Receptors and the Link Between Innate and Adaptive Immunity. 7.
Chemical synthesis of tumor-associated carbohydrates and glycopeptides. 8.
Semi-synthetic carbohydrate-based cancer vaccines. 9. Fully synthetic
carbohydrate-based cancer vaccines. 10. B-epitope and receptor ligand
di-epitope constructs. 11. B- and T-cell di-epitope constructs. 12.
Tri-component vaccines. References. Chapter 10: Glycoengineering of Cell
Surface Sialic Acid and Its Application to Cancer Immunotherapy (Zhongwu
Guo). 1. Introduction. 2. Engineering of Cell Surface Sialic Acids. 3.
Sialic Acid engineering for Modulation of Cell Surface Reactivity. 4.
Sialic Acids engineering for Cancer Immunotherapy. 5. Summary.
Acknowledgement. References Cited. Chapter 11: Therapeutic Cancer Vaccines:
Clinical Trials and Applications (Hans H. Wandall and Mads A. Tarp). 1.
Introduction. 2. Innate and adaptive immunity in relation to cancer
immunotherapy. 3. Design issues for clinical cancer vaccine trials. 4.
Clinical development of cancer vaccines. 5. Proof of principle trials. 5.1
Toxicity and pharmacokinetics. 5.2 Dose and administration schedule. 5.3
Endpoints: Biological activity and clinical activity. 6. Efficacy Trials.
7. Clinical endpoints in efficacy trials. 8. Challenges in vaccine
development. 9. Defining the target tumor-associated antigens. 10.
Production and storage issues. 11. Clinical trials. 11.1
Glycosphingolipid-based vaccines. 11.2 O-glycan-based vaccines. 12.
Conclusions. Acknowledgement. References Cited. Chapter 12: Carbohydrates
as Unique Structures for Disease Diagnosis (Kate Rittenhouse-Olson). 1.
Introduction. 2. Viruses. 2.1 Infectious mononucleosis. 2.2 Influenza A and
B. 3. Bacteria. 3.1 Streptococcus pyogenes. 3.2 Groups A, B, C, D, F and G
Streptococcus. 3.3 Streptococcus pneumoniae. 3.4 Meningitis. 3.5 Chlamydia
trachomatis. 3.6 Future. 4. Fungi. 4.1 Aspergillus fumigatus. 4.2 Invasive
Candidiasis. 4.3 Cryptococcus neoformans. 4.4 Histoplasma capsulatum. 5.
Parasites. 5.1 Echinococcus multilocularis. 5.2 Clonorchis sinensis. 5.3
Trichinella. 5.4 Schistomsoma mansoni. 6. Autoimmunity. 6.1 Diabetes. 6.2
Cold agglutinin disease. 6.3 Inflammatory bowel disease. 7. Tumors. 7.1
Bladder. 7.2 Breast. 7.3 Colon. 7.4 Liver. 7.5 Lung. 7.6 Melanoma. 7.7
Ovarian. 7.8 Pancreatic. 7.9 Prostate. 8. Inherited or acquired disorders
of glycosylation. References Cited.