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From Lymphatic System
MALT
Mucosa-associated lymphoid tissue.
1. Overview
Mucosa-associated lymphoid tissue (MALT) refers to a collection of diffuse and organized lymphoid tissues located within mucosal surfaces throughout the body. As part of the immune system, MALT plays a crucial role in defending against pathogens that enter through mucosal barriers such as the respiratory, gastrointestinal, and genitourinary tracts. It houses immune cells that detect, respond to, and eliminate invading microorganisms while helping maintain immune tolerance to harmless antigens like food and commensal bacteria.
2. Location
MALT is distributed throughout various mucosal sites of the body, forming the largest component of the lymphatic system. It is categorized based on its location:
GALT (Gut-associated lymphoid tissue): Found in the gastrointestinal tract (e.g., Peyer’s patches, appendix, tonsils, isolated lymphoid follicles).
BALT (Bronchus-associated lymphoid tissue): Located in the respiratory tract, especially around bronchi and bronchioles.
NALT (Nasal-associated lymphoid tissue): Present in the nasal passages, particularly in the adenoids.
VALT (Vulvovaginal-associated lymphoid tissue): Found in the female reproductive tract.
Other locations: Salivary glands, lacrimal glands, conjunctiva, and urinary tract mucosa.
Unlike lymph nodes, MALT is not always encapsulated and may appear as diffuse lymphoid aggregates interspersed within the mucosal epithelium and lamina propria.
3. Structure
MALT includes both organized and diffuse lymphoid tissues, structurally designed to interact closely with the mucosal surface. Its components include:
Epithelium-associated lymphocytes: Lymphocytes scattered within or beneath the mucosal epithelium.
Lymphoid follicles: Contain B cells in germinal centers surrounded by T cells and antigen-presenting cells (e.g., dendritic cells, macrophages).
Specialized epithelial cells: M cells (microfold cells) transport luminal antigens across the epithelium into lymphoid tissue below.
Plasma cells: Produce immunoglobulin A (IgA), which is secreted into the mucosal surface to neutralize pathogens.
MALT lacks a fibrous capsule (unlike lymph nodes) and is instead closely integrated with the mucosal epithelium, allowing immediate immune responses to local stimuli.
4. Function
MALT functions as the body’s first line of defense at mucosal surfaces. Its major functions include:
Antigen sampling: M cells and dendritic cells capture pathogens and antigens from the mucosal surface and deliver them to immune cells.
Immune response initiation: Activates T and B lymphocytes in response to foreign antigens.
Antibody production: Promotes class switching of B cells to secrete IgA, which is critical for mucosal immunity.
Maintenance of immune tolerance: Helps suppress immune responses to non-threatening antigens like food proteins and commensal microbes.
5. Physiological Role(s)
MALT plays vital roles in both immunity and immune regulation, especially at mucosal interfaces. These roles include:
Barrier immunity: Prevents pathogen entry by initiating rapid localized immune responses at mucosal surfaces.
Regulation of inflammation: Balances pro-inflammatory and anti-inflammatory signals to protect mucosal tissues from chronic damage.
Oral tolerance: Facilitates immunological unresponsiveness to harmless antigens, preventing allergic or autoimmune reactions.
Immune education: Particularly during childhood, MALT exposes immune cells to diverse antigens, helping shape immune memory.
6. Clinical Significance
Infections
MALT is a primary site of defense against mucosal pathogens, including viruses, bacteria, and parasites. Dysfunction or depletion of MALT (e.g., in HIV infection) compromises mucosal immunity, increasing susceptibility to infections in the gut, lungs, and genital tract.
Autoimmune and Inflammatory Disorders
Inflammatory bowel disease (IBD): Aberrant activation of GALT contributes to the pathogenesis of Crohn’s disease and ulcerative colitis.
Celiac disease: Loss of tolerance to gluten in GALT results in villous atrophy and chronic inflammation of the small intestine.
Asthma and allergic rhinitis: BALT and NALT play roles in hypersensitivity reactions to inhaled allergens.
MALT Lymphoma
MALT lymphomas are extranodal marginal zone B-cell lymphomas that arise from chronic antigenic stimulation in MALT. Common sites include:
Stomach: Associated with chronic Helicobacter pylori infection.
Salivary glands: Linked to Sjögren’s syndrome.
Thyroid: Often related to Hashimoto’s thyroiditis.
Treatment often includes eradication of the underlying infection or autoimmune trigger, in addition to radiation or immunotherapy.
Vaccination and Immunotherapy
MALT is an important target for mucosal vaccines, such as oral polio vaccine and nasal influenza vaccines. These vaccines stimulate MALT directly to produce localized immunity, especially secretory IgA, enhancing protection at pathogen entry points.
Did you know? Lymphangitis is an inflammation of the lymphatic vessels that often occurs due to an infection.