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Asian Journal of Immunology

Asian Journal of Immunology, ..,Vol.: 1, Issue.: 1

Review Article

The Martyrdom of St. Julia: On Microbial Strategies to Evade the Immune System


Thuc Anh Nguyen1, Angkarina Angkasuwan1, Claudia Rossi1, Frans J. Van Overveld1 and Ger T. Rijkers1,2*

1Department of Science, University College Roosevelt, Lange Noordstraat 1, 4331 CB Middelburg, The Netherlands.

2Laboratory of Medical Microbiology and Immunology, St. Antonius Hospital, Nieuwegein, The Netherlands.


Article Information


(1) Jaffu Othniel Chilongola, Department of Biochemistry and Molecular Biology, Kilimanjaro Christian Medical University College, Tumaini University, Tanzania.


(1) Tania Mara Pinto Dabés Guimarães, Federal University of Minas Gerais, Brazil.

(2) Festus Otajevwo, Western Delta University, Nigeria.

(3) M. Zamri Saad, Universiti Putra Malaysia, Malaysia.

Complete Peer review History: http://www.sciencedomain.org/review-history/24615




Bacteria and viruses use an array of evasion mechanisms to escape from the host immune system. Due to antigenic variation, pathogenic micro-organisms can escape the immune system. Micro-organisms can occur in different types, such as the 97 serotypes of Streptococcus pneumoniae. Influenza viruses change their antigenic make-up, in particular, the hemagglutinin molecule by antigenic drift and antigenic shift. Trypanosomes and malaria parasites use DNA programmed expression of highly variable surface antigens. Micro-organisms can also produce proteins that degrade (IgA protease) or inactivate antibody molecules (protein A and protein G). Some bacteria and viruses produce proteins that inhibit complement activation. Virus can become invisible for recognition by T-lymphocytes by interference with antigen presentation. Antiviral immunity can be suppressed by viral homologues of cytokines and cytokine receptors and other proteins. Despite the extensive immune evasion strategies used by viruses, bacteria and other micro-organisms, the immune system in most cases is ultimately able to control an infection.


Keywords :

Evasion mechanisms; IgA proteases; capsular polysaccharides; antigenic drift; antigenic shift; complement inhibitors; antigen presentation; cytokine homologues.


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