Class 12 Biology Notes
Complete, exam-ready notes on human health and disease: major communicable diseases and their causative agents, the immune system (innate, acquired, humoral and cell-mediated), vaccination, cancer biology, AIDS, and the effects of drugs and alcohol abuse. Vital for CBSE Class 12 and NEET Biology.
Written byDeep Narayan· Science & Mathematics EducatorReviewed byPushpanjali
Humoral immunity (B-lymphocyte-mediated, antibody response) and cell-mediated immunity (T-lymphocyte-mediated, destroys infected cells directly).
Communicable diseases are caused by pathogens — bacteria, viruses, protozoans, helminths and fungi — transmitted through contaminated food, water, air or vectors.
Malaria — know the full story
Malaria is caused by Plasmodium species: P. vivax (benign tertian), P. malariae (quartan), P. ovale (benign tertian) and P. falciparum (malignant tertian — most deadly). The female Anopheles mosquito is the vector. Inside the human liver, sporozoites multiply into merozoites, which infect RBCs, causing their rupture and the characteristic periodic fever.
Plasmodium vivax life cycle: Sporozoites from mosquito bite → liver cells (exo-erythrocytic schizogony) → merozoites released into blood → infect RBCs (erythrocytic schizogony) → RBCs rupture releasing merozoites and toxins → periodic fever every 48 hours. Some merozoites develop into gametocytes, which are picked up by a female Anopheles mosquito to continue the cycle.
The ability of the body to resist or fight disease-causing organisms. It is broadly divided into innate (non-specific, present from birth) and acquired (specific, developed after exposure).
In the primary response, B-cells are activated by an antigen, proliferate and differentiate into plasma cells (which secrete antibodies) and memory cells. The response is slow (latent period). In the secondary response, upon re-exposure, memory cells recognise the antigen rapidly, producing a faster, stronger and longer-lasting antibody response.
B-lymphocytes mature in the bone marrow and mediate humoral immunity by producing antibodies (immunoglobulins — IgG, IgA, IgM, IgD, IgE). T-lymphocytes mature in the thymus and mediate cell-mediated immunity: helper T-cells (CD4) activate B-cells and other T-cells; cytotoxic T-cells (CD8) directly kill infected cells; suppressor T-cells regulate the immune response.
Antigen-antibody specificity
Each antibody has a variable region that fits a specific epitope (antigenic determinant) on the antigen, like a lock and key. Antibodies do not kill pathogens directly — they neutralise toxins, opsonise (mark) pathogens for phagocytosis, and activate complement.
Administration of antigens (weakened/killed pathogens, toxoids, mRNA or recombinant proteins) to stimulate primary immune response and generate memory cells, without causing the disease. Booster doses reinforce the secondary response.
An exaggerated immune response to harmless environmental substances (allergens — pollen, dust mites, certain foods). IgE antibodies are produced; they bind to mast cells, which release histamine upon re-exposure, causing sneezing, runny nose, skin rash. Treatment: antihistamines.
The immune system mistakenly attacks the body's own cells. Examples: rheumatoid arthritis (joints), Type 1 diabetes (pancreatic beta cells), myasthenia gravis (neuromuscular junctions), systemic lupus erythematosus (multiple organs).
Uncontrolled, abnormal cell growth that can spread to other tissues (metastasis). Cancer cells divide without normal growth regulation due to mutations in proto-oncogenes, tumour suppressor genes or DNA repair genes.
A late-stage, life-threatening condition caused by Human Immunodeficiency Virus (HIV), a retrovirus (RNA virus). HIV selectively infects and destroys CD4+ helper T-cells, progressively destroying the immune system and leaving the body vulnerable to opportunistic infections and certain cancers (Kaposi's sarcoma, lymphomas).
Substance abuse refers to the harmful use of psychoactive drugs and alcohol, leading to physical dependence, tolerance and withdrawal symptoms. Major categories relevant to NCERT:
Prevention is better than cure
Preventive measures: avoid peer pressure, seek counselling, engage in healthy activities, proper disposal of unused medicines, strict regulation of sale. India's NDPS Act (Narcotic Drugs and Psychotropic Substances) controls production and distribution of these substances.
Example: A patient shows recurrent episodes of fever with chills every 48 hours. Blood smear reveals ring-stage parasites in RBCs. Identify the most likely Plasmodium species, the vector and one diagnostic test.
Solution: Fever every 48 hours (tertian periodicity) with ring-stage parasites in RBCs points to Plasmodium vivax (benign tertian malaria). The vector is the female Anopheles mosquito. Diagnostic methods include blood smear examination under a microscope (stained with Giemsa stain) to detect the parasite, or the rapid diagnostic test (RDT) based on HRP2 antigen.
Example: Distinguish between active immunity and passive immunity with one example each.
Solution: Active immunity involves the body producing its own antibodies after exposure to an antigen, providing long-lasting memory — example: recovering from chickenpox gives lifelong immunity. Passive immunity involves receiving ready-made antibodies from another source, providing immediate but temporary protection — example: a mother transfers IgA antibodies to her infant through breast milk.
Revision
Memorise these before attempting numericals — most exam questions hinge on one of them.
Primary vs secondary response
Antibody classes
Diploid number
CD4/CD8 ratio
T-cell maturation
IgE in allergy
Cancer cell property
Exam tips
Where this topic appears in CBSE, JEE Main and NEET papers.
FAQ
Innate immunity is non-specific and present from birth (skin, phagocytes, inflammation). Acquired immunity is specific, develops after exposure to antigens, and has memory (humoral and cell-mediated responses).
HIV infects CD4+ helper T-cells using the CD4 receptor and CCR5/CXCR4 co-receptors. Inside the cell, reverse transcriptase converts viral RNA into DNA, which integrates into the host genome. Progressive destruction of helper T-cells collapses the immune response, leading to AIDS.
Benign tumours remain localised, grow slowly and do not spread. Malignant tumours invade surrounding tissues and metastasise to distant organs via blood or lymph, making them far more dangerous and harder to treat.
Booster doses re-expose the immune system to the antigen, stimulating memory cells to mount a rapid and robust secondary response. This ensures sustained high antibody levels and long-term protection.
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