2. Describe the immunoserological characteristics of a hepatitis B-related antigen. 3. Describe the immunoserological characteristics of a hepatitis B - surface antigen.
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- 3. Describe the immunoserological characteristics of a hepatitis B - surface antigen.Shortly discuss the different immunodeficiency and immunoproliferative disorders and include the following: a. General Characteristic b. Cause c. Signs and Symptoms d. Clinical Diagnosis and Clinical Picture e. Immunologic Manifestations f. Treatment.VI. Match each of the following lymphoid organs with its correct description. a. lymphatic vessels b. tonsils c. lymph nodes d. spleen e. thymus 1. largest lymphatic organ 2. transport lymph 3. filter lymph 4. atrophies with age 5. located in the pharynx Examining the Histology of a Lymph Node, a Tonsil, and the Spleen Which lymphoid organ: a. contains red pulp and white pulp? b. contains more afferent vessels than efferent vessels? c. lacks a capsule? d. contains crypts? e. contains an outer cortex and an inner medulla?
- 1. How does HBV virus differ from other hepatitis B viruses?2. What are other HBV antigens?3. What is the diagnostic significance of each of these antigens?4. What is the function of surface antigen of the HB virus?5. Could somebody with HBV infection recover from the disease? Explain your answer.4) Identify how neoplastic cells might come to the attention of the immune system.1- A. Define the term pathogen. B. Using MRSA, NOROVIRUS, ATHLETES FOOT and MALARIA as examples, identify the microorganisms (causal agent) involved in each disease. C. Provide some information on the microorganism for each disease e.g. structure D. Discuss 3 routes of entry that disease causing organisms use to enter the body.
- 3) Describe how neoplastic cells challenge the tissue around them. 4) Identify how neoplastic cells might come to the attention of the immune system.1. What are the functions/basic anatomy and physiology of antibodies? Please include citation (s)a. Explain why babies with agammaglobulinemia do not developopportunistic infections until about 6 months after birth.b. Explain why people with B-cell deficiencies can benefit fromartificial passive immunotherapy. Explain whether vaccinationwould work for them.c. Explain why T-cell deficiencies usually cause more severe effectsthan B-cell deficiencies.