Pathogens are disease-causing agents that disrupt normal physiology.
They can be cellular (bacteria, fungi, parasites) or non-cellular (viruses, prions).
Viruses insert genetic material into host cells to multiply.
Prions are infectious proteins with abnormal folding.
Bacteria reproduce quickly and compete with host cells.
Fungi colonize body surfaces.
Parasites feed on a host (microparasites/protozoa or macroparasites/helminths).
First line: Surface barriers prevent pathogen entry.
Second line: Non-specific defenses activated after infection.
Third line: Specific responses target antigens from pathogens.
Physical barriers: obstruct access (e.g., skin, mucous membranes).
Chemical barriers: hinder survival via chemical compounds (e.g., gastric secretions, sweat).
Microbiological barriers: Natural flora prevent colonization.
Restores intact external layer when surface barriers are penetrated.
Initiated by clotting factors from damaged cells/platelets.
Prothrombin converts to thrombin, fibrinogen to fibrin, forming a clot.
Non-specific defense; responds the same way every time.
Phagocytic leukocytes internalize and digest pathogens.
Phagocytes recruited by chemotactic chemicals.
Lymphatic system filters fluid (lymph) and removes pathogens.
Antigen-presenting cells (APCs) transport antigens to lymphocytes.
Specific defense; recognizes specific antigens.
Produces heightened response upon re-exposure (immunological memory).
Lymphocytes in lymph nodes are principal components.
Molecular markers on pathogen surfaces.
Targeted by antibodies.
B and T lymphocytes recognize specific antigens.
Clonal selection/expansion: lymphocyte activated to divide & form clones.
Helper T cells coordinate adaptive response, activate B lymphocytes.
B cells form plasma cells (produce antibodies) and memory cells.
Proteins produced by B lymphocytes specific to an antigen.
Y-shaped molecules with variable regions for antigen specificity.
Facilitate pathogen destruction via opsonization, etc.
Produced when B and T lymphocytes divide.
Enable faster, more potent secondary immune response.
Provide immunological memory and immunity.
Compromised or absent immune system.
HIV infects helper T lymphocytes, leading to AIDS.
Transmitted via bodily fluids.
Target prokaryotic features in bacteria.
Antibiotic resistance develops via mutations and gene transfer.
Injection of attenuated pathogens/antigenic fragments to provide active acquired immunity.
Initiates primary response and memory cell production.
Secondary response prevents disease symptoms upon exposure.
Indirectly protects non-vaccinated individuals when a large percentage of population is immune.
Limits pathogen spread.
Epidemic: outbreak in a community/region.
Pandemic: outbreak across a wider geographical area.