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The Biology of Dendritic Cells and HIV Infection

معرفی کتاب «The Biology of Dendritic Cells and HIV Infection» نوشتهٔ Sandra Gessani; ‎Filippo Belardelli، منتشرشده توسط نشر Springer Science+Business Media در سال 2007. این کتاب در فرمت pdf، زبان انگلیسی ارائه شده است.

Dendritic cells play the most vital part in inducing anti-viral immune responses in HIV and AIDS among many other viruses. Research on dendritic cells (DCs) is emerging as a fundamental aspect for the comprehension of the mechanisms underlying the pathogenesis of viral diseases as well as for the progress on the development of prophylactic and therapeutic vaccines. This volume focuses on the role of DCs in the pathogenesis and immunity of HIV-1 infection. It has recently been clarified that DCs are important targets and reservoirs of HIV and may play an important role in virus spreading to T cells. Interestingly, HIV can exploit many of the cellular processes responsible for the generation and regulation of the adaptive immune responses to gain access to its main target cells, i.e. the CD4 + T lymphocytes. Thus, the central role of DCs in stimulating T cell activation not only provides a route for viral transmission, but also represents a vulnerable point at which HIV-1 can interfere with the initiation of primary T cell immunity. Recent studies have revealed that several HIV proteins can profoundly influence the phenotype and functions of DCs even in the absence of a productive infection, often resulting in an abnormal immune response. While this knowledge has resulted in the identification of some major mechanisms involved in the pathogenesis of HIV-1 infection, the recent progress on DC biology has opened perspectives in the research on new adjuvants (selectively acting on DCs) and on novel strategies for the in vivo targeting of antigens to DCs, which appear to be highly relevant for the development of HIV vaccines. Of note, defects in the number and functions of DCs have been observed in the course of HIV infection and during disease progression, thus suggesting that DCs play an important role in the immune control of viral replication and virus-induced dysfunctions. The development of therapeutic vaccination strategies to be combined with HAART is thought as an important step for an effective control of HIV infection in patients. In this context, the use of autologous DCs may represent an attracting strategy. Notably, DCs are now regarded as a valuable approach for the development of cancer vaccines and several clinical trials have explored the efficacy of different DC preparations as cellular adjuvants in inducing a potentially protective immune response. Recent data in animal models provide the background for the clinical testing of DC-based vaccines in HIV-1-infected patients. Now that we start to understand the complex interactions between HIV and DCs in the pathogenesis of AIDS and we are learning how to prepare potentially effective DCs from lessons on cancer vaccines, we may reasonably assume that DC-based therapeutic vaccines can represent a topic of increasing interest in protocols of clinical immunotherapy of HIV-1-infected patients.

dendritic Cells Play The Most Vital Part In Inducing Anti-viral Immune Responses In Hiv And Aids Among Many Other Viruses. Research On Dendritic Cells (dcs) Is Emerging As A Fundamental Aspect For The Comprehension Of The Mechanisms Underlying The Pathogenesis Of Viral Diseases As Well As For The Progress On The Development Of Prophylactic And Therapeutic Vaccines.

this Volume Focuses On The Role Of Dcs In The Pathogenesis And Immunity Of Hiv-1 Infection. It Has Recently Been Clarified That Dcs Are Important Targets And Reservoirs Of Hiv And May Play An Important Role In Virus Spreading To T Cells. Interestingly, Hiv Can Exploit Many Of The Cellular Processes Responsible For The Generation And Regulation Of The Adaptive Immune Responses To Gain Access To Its Main Target Cells, I.e. The Cd4+ T Lymphocytes. Thus, The Central Role Of Dcs In Stimulating T Cell Activation Not Only Provides A Route For Viral Transmission, But Also Represents A Vulnerable Point At Which Hiv-1 Can Interfere With The Initiation Of Primary T Cell Immunity.

recent Studies Have Revealed That Several Hiv Proteins Can Profoundly Influence The Phenotype And Functions Of Dcs Even In The Absence Of A Productive Infection, Often Resulting In An Abnormal Immune Response. While This Knowledge Has Resulted In The Identification Of Some Major Mechanisms Involved In The Pathogenesis Of Hiv-1 Infection, The Recent Progress On Dc Biology Has Opened Perspectives In The Research On New Adjuvants (selectively Acting On Dcs) And On Novel Strategies For The In Vivo Targeting Of Antigens To Dcs, Which Appear To Be Highly Relevant For The Development Of Hiv Vaccines. Of Note, Defects In The Number And Functions Of Dcs Have Been Observed In The Course Of Hiv Infection And During Disease Progression, Thus Suggesting That Dcs Play An Important Role In The Immune Control Of Viral Replication And Virus-induced Dysfunctions. The Development Of Therapeutic Vaccination Strategies To Be Combined With Haart Is Thought As An Important Step For An Effective Control Of Hiv Infection In Patients. In This Context, The Use Of Autologous Dcs May Represent An Attracting Strategy. Notably, Dcs Are Now Regarded As A Valuable Approach For The Development Of Cancer Vaccines And Several Clinical Trials Have Explored The Efficacy Of Different Dc Preparations As Cellular Adjuvants In Inducing A Potentially Protective Immune Response. Recent Data In Animal Models Provide The Background For The Clinical Testing Of Dc-based Vaccines In Hiv-1-infected Patients. Now That We Start To Understand The Complex Interactions Between Hiv And Dcs In The Pathogenesis Of Aids And We Are Learning How To Prepare Potentially Effective Dcs From Lessons On Cancer Vaccines, We May Reasonably Assume That Dc-based Therapeutic Vaccines Can Represent A Topic Of Increasing Interest In Protocols Of Clinical Immunotherapy Of Hiv-1-infected Patients.

General aspects of dendritic cell biology, functions, and clinical application. Dendritic cell biology: subset heterogeneity and functional plasticity / Vassili Soumelis, Yong-Jun Liu, and Michel Gilliet. Dendritic cells and their role in linking innate and adaptive immune responses / Mary F. Lipscomb, Julie A. Wilder, and Barbara J. Masten. Dendritic cell and pathogen interactions in the subversion of protective immunity / John E. Connolly, Damien Chaussabel, and Jacques Banchereau. Dendritic cells as keepers of peripheral tolerance / Sabine Ring, Alexander H. Enk, and Karsten Mahnke. Adjuvants, dendritic cells, and cytokines: strategies for enhancing vaccine efficacy / Paola Rizza, Imerio Capone, and Filippo Belardelli. Ex vivo-generated dendritic cells for clinical trials versus in vivo targeting to dendritic cells: critical issues / Joannes F.M. Jacobs ... [et al.] -- General aspects of the pathogenesis and immune response to HIV-1 infection. Immunopathogenesis of HIV infection / Elisa Vicenzi ... [et al.] Innate cellular immune responses in HIV infection / Barbara Schmidt ... [et al.] Adaptive immune responses in HIV-1 infection / Mara Biasin and Mario Clerici -- Dendritic cells and HIV interactions and their role in pathogenesis and immunity. Binding and uptake of HIV by dendritic cells and transfer to T lymphocytes: implications for pathogenesis / Anthony L. Cunningham ... [et al.] Loss, infection, and dysfunction of dendritic cells in HIV infection / Steven Patterson, Heather Donaghy, and Peter Kelleher. HIV exploitation of DC biology to subvert the host immune response / Manuela Del Cornò ... [et al.] Cross-presentation by dendritic cells: role in HIV immunity and pathogenesis / Concepción Marañón ... [et al.] Immunotherapy of HIV infection: dendritic cells as targets and tools / Imerio Capone ... [et al.]
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