BIO Laboratory #7: Immunology

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BIO 111 - Laboratory #7: Immunology Assigned pages: "Biology Project Immunology" Handout (in numbered manila folder) Please, RETURN THE FOLDER, at the end of class, when you are finished Additional information is available in your lecture text (C. Starr and R. Taggert. 2008. Biology - The Unity and Diversity of Life, SUNY Cortland edition, 11th edition. Mason, OH: Thompson Custom Solutions) on pages 678-699. Website used as a source for this lab: Introduction to Immunology - Great site with live video clips: http://www.biology.arizona.edu/immunology/tutorials/immunology/main.html HAND IN BOTH worksheets - Answer the assigned, 12 multiple choice questions (max., 6 points) I. Immunology: 1. GOALS: Objectives - at the end of laboratory #7 you should be able to: 1.) state the major functions of immune system 2.) list the functions of each part of the immune system - thymus, white blood cells, antibodies, epidermis, cilia, mucus, and saliva. 3.) describe the interaction between antibodies and antigens 4.) compare and contrast the innate (nonspecific) responses with adaptive (specific) immunity responses of the human body 5.) compare and contrast humoral immunity (initiated by B cells) with cell-mediated immunity (initiated by T cells) within the adaptive (specific) immune response 6.) describe the actions of helper T cells and cytotoxic T cells 7.) explain how bodies develop immunity against disease 8.) briefly define HIV (an RNA virus), AIDS, and how HIV is transmitted 9.) know the function of AZT and "protease inhibitors" in fighting AIDS Key terms - you should be able to define: pathogen nonspecific defenses macrophages phagocytosis vs. cell lysis complement proteins inflammatory response histamine lymphocytes antigen vs. antigen presenting cells antibody antigen receptors lymphatic system immunity humoral immunity cell-mediated immunity memory cells effector cells cytotoxic T cells helper T cells B cells self/ non-self recognition complex vaccination I. Immunology - Introduction to Major Concepts 1. Immunology Manual Handout: 1.) Read: pp. 1-7, 9, 10-11, 12, and 13 (section numbers correspond to number of question) 2. Immunology Worksheet: 1.) Answer: questions 1-4, 7, 9, 11, and 13 (one half point each) 2.) Read review pages and hand in the worksheet, at the end of class 3. Review : Read pp. 25-26. II. HIV/ AIDS - Epidemic and Impacts 1. Immunology Manual Handout: 1.) Read: pp. 17-21, and 23-24 (section numbers correspond to number of question) 2. HIV/AIDS Worksheet: 1.) Answer: questions 1,2, 5, and 6 (one half point each) 2.) Read review pages and hand in the worksheet, at the end of class 3. Review: Read pp. 27-30

BIO 111 - Laboratory #7: Immunology Introduction -WORKSHEET - ANSWER assigned questions only and HAND IN at the end of this lab, please. NAME (PRINT, clearly): Day of your lab: Time of your lab: Using the information provided in the handout, please, answer the following questions (one half point each): 1. A pathogen is a type of antigen? A. True B. False 2. Expectant parents now have the option to save their baby's "cord blood" (blood from the umbilical cord) immediately following birth. This cord blood can be transplanted into individuals whose blood has been damaged by diseases such as leukemia, Hodgkin's lymphoma, and sickle cell anemia. Saved cord blood is a perfect match for the baby it came from, and can also be useful in treating relatives of the baby. What cells should be harvested from the cord blood to best treat patients with blood diseases? A. Erythrocytes (red blood cells) B. Leukocytes (granulocytes, monocytes, and lymphocytes) C. Stem cells 3. Immediately following a break in the skin, phagocytes engulf bacteria within the wound. This is an example of an immune response which is against a pathogen. A. adaptive, specific C. innate, nonspecific B. innate, specific D. adaptive, nonspecific 4. are responsible for the production of antibody against free pathogens and soluble products from pathogens while destroy pathogens, virally infected cells, and abnormal cells. A. Cytotoxic T cells, B cells C. B cells, helper T cells B. Macrophages, T cells D. B cells, cytotoxic T cells 5. The ability to produce billions of different antibodies in humans results from: A. The presence of billions of complete antibody genes in B cells. B. The fact that both T cells and B cells contain antibody genes. C. The production of variable regions of light and heavy antibody genes by DNA rearrangement.

D. The fact that a single antibody gene produces an antibody capable of billions of different threedimensional structures and the ability to combine with any antigen. 6. If a B cell clone began to produce antibody with altered binding strength and specificity for antigen, you would expect the mutation of the antibody gene to involve: A. The variable region of the heavy chain or the constant region of the light chain B. The variable region of the light chain or the constant region of the heavy chain C. The variable regions of the light or heavy chains D. The constant regions of the light or heavy chains 7. Allergies result from the production of directed against an antigen. A. IgG B. IgA C. IgM D. IgE 8. Epstein Barr virus (EBV) infects endothelial cells and B cells. About half of us are infected by the virus while very young, and do not suffer disease. Around half of individuals who avoid the virus while young are infected in the teenage years and develop a disease called mononucleosis. In this disease, lymph nodes swell painfully as our immune system produces large numbers of lymphocytes to eliminate virus-producing cells. These lymphocytes are probably: A. B cells which produce antibody eliminating virus-infected cells B. Cytotoxic T cells to destroy virus-containing cells C. Helper T cells which stimulate B cell clonal selection D. Granulocytes which invade areas of virus production 9. The clonal selection theory of antibody diversity says: A. B cell precursors randomly rearrange variable coding parts of antibody genes. Afterwards, antigen binds to a clone with specific membrane antibody, resulting in differentiation to antibody secreting plasma cells B. The antigen causes a nonspecific clone of B lymphocytes to proliferate and secrete antibody molecules capable of binding to any foreign antigen C. Antigen causes the growth of a clone of lymphocytes which then rearrange DNA, creating a gene coding for a specific antibody D. A clone of macrophages with specific receptor for antigen phagocytoses antigen, then rearranges DNA to generate specific antibody-coding genes 10. The significance of the major histocompatibility complex (MHC) in the immune response: A. Serves to minimize autoimmunity or "self-reactivity" of the immune system B. Serves to present fragments of antigens to T-cells.

C. Used by helper T-cells to regulate the expansion of antibody producing B-cells. D. All of the above. 11. The lack of an immune response to self is called: A. Autoimmunity B. Tolerance 12. Human HLA genes (equivalent to MHC genes in mice) have many alleles, and no two individuals have identical alleles at all gene loci. Which of the following are consequences of this genetic diversity? A. Maximizes the kinds of pathogens that can be recognized and eliminated by an immune response within a population B. Transplanted organs can be rejected C. Females mice prefer to mate with males having different alleles at MHC gene loci D. All of the above. 13. Monoclonal antibodies come from clones of B cells that produce a single antibody of known specificity. B cells will nor normally divide in the absence of antibody. The special trick that allowed monoclonal antibody-producing cells to be grown in culture was: A. Mice were immunized with antigen and T cells removed and grown in culture to produce antibody B. Mice were injected with antigen and B cells were fused with cancer cells, producing a hybrid cell line that can grow in culture yet still produce antibody against the antigen C. Antibodies were produced by isolating mrna from immunized mice and translating the message for antibody in the laboratory D. Macrophages were isolated from immunized mice that would stimulate naive B cells to continue to divide in culture, allowing the production of monoclonal antibodies

BIO 111 - Laboratory #7: HIV/ AIDS -WORKSHEET - ANSWER assigned questions only and HAND IN at the end of this lab, please. NAME (PRINT, clearly): Day of your lab: Time of your lab: Using the information provided in the handout, please, answer the following questions (one half point each): 1. Which HIV+ patient is most likely to have AIDS? (Circle one answer) A. A person who engaged in high-risk sexual behavior three months ago B. A person who engaged in high-risk sexual behavior ten years ago C. A recently infected person whose drug therapies include reverse transcription inhibitors and protease inhibitors D. A person who has an almost normal number of helper T cells detected in her blood sample 2. Which activity has a high risk of HIV transmission? (Circle one answer) A. Living with someone who is HIV+ B. Receiving a blood transfusion today, with blood that has been screened for HIV C. Sexual intercourse without a condom D. Working as a paramedic 3. Which immune response is specific against one antigen? (Circle one answer) A. Skin blocks entry of antigen into body B. Phagocytic cell engulfs antigen C. Antibody binds antigen and prevents it from infecting cells D. Cilia sweep antigens away from lungs 4. What type of specialized white blood cell interacts with other cells, regulating the production of antibodies and destruction of infected cells? (Circle one answer) A. B cells B. Helper T cells C. Cytotoxic T cells D. Phagocytes 5. AZT, a reverse transcription inhibitor, stops HIV reproduction at what stage? (Circle one answer) A. Producing viral DNA from RNA B. Translating RNA into protein C. Producing viral and host DNA from RNA D. Integrating viral DNA into host DNA 6. Protease inhibitors prevent: (Circle one answer) A. HIV attachment to helper T cells B. Reverse transcription of viral RNA C. Integration of viral DNA into host DNA D. Cutting of a large protein (polypeptide) into multiple smaller proteins essential for viral reproduction