박테리아 병원균에 대한 방어

Macrophages are non-specific phagocytes that recognize and engulf diverse bacterial cells without prior sensitization. B cells, by contrast, recognize only specific bacterial antigens corresponding to their unique antigen receptors. Both cells function as antigen-presenting cells, processing bacterial antigens and displaying them using MHC molecules to activate T cells.

Helper T cells differentiate from naive CD4 T cells after antigen presentation by APCs. These effector cells release cytokines that stimulate B cells to proliferate and differentiate into antibody-producing plasma cells. Cytokines also enhance macrophage phagocytosis, amplifying the overall immune response against bacterial infections.

Opsonization occurs when antibody molecules form complexes with bacterial antigens, coating the bacterial cell surface with antibodies. This antibody coating marks bacteria for destruction and significantly enhances their recognition and uptake by phagocytic cells like macrophages and neutrophils, accelerating bacterial clearance.

When bacteria infect host cells, infected cells present bacterial antigens complexed with MHC I molecules to naive CD8 T cells. These cells differentiate into cytotoxic T cells, which recognize the presented antigens and kill infected cells by releasing cytotoxic molecules that induce apoptosis, eliminating the intracellular bacterial threat.

Mycobacterium tuberculosis has evolved intricate cell wall structures that resist the digestive enzymes within macrophage lysosomes, allowing the bacteria to survive intracellularly. This resistance enables the pathogen to persist and cause chronic infections. Such evasion mechanisms result from natural selection and evolutionary adaptation rather than conscious pathogen strategies.

Methicillin-resistant Staphylococcus aureus has developed resistance to multiple antibiotics, making infections difficult to treat. Additionally, different bacterial strains feature different surface antigens, so an immune response effective against one strain may not protect against another. This antigenic variation allows bacterial species to survive and adapt despite immune pressure.

When confronted with resistant bacteria, macrophages activated by cytokine signals from helper T cells engage specialized metabolic pathways involving oxidative metabolism. These pathways create an inhospitable environment for bacteria, often employing nitric oxide to eliminate the pathogen within the macrophage, overcoming lysosomal enzyme resistance.