IMMUN: Respiratory Immunology Flashcards
what does BALT stand for and where is it located within the tissue?
- bronchus-associated lymphoid tissue
- located in lamina propria
what does the lamina propria contain? (immune wise)
- BALT
- plasma cells
- Tc cells
- macrophages
- mast cells
mucociliary escalator
- goblet cells in epithelium secrete mucus
- cilia (pseudostratified ciliated columnar epithelium) beat in an asymmetric rhythm
- mucus moves 1cm/minute
what can interfere with the mucociliary escalator
- smoking
- anaesthetic
- infection
- immotile cilia syndrome
- CF (makes mucus thicker)
function of respiratory epithelial cells
- express PRRs which recognise PAMPs
- secrete chemokines and cytokines to recruit immune cells
- secrete antimicrobial compounds e.g. defensins into the lumen of the airway
two types of lung macrophages
- alveolar: phagocytose inhaled particles
- interstitial: activated if epithelial barrier is breached
why are neutrophils a good inflammatory marker?
- in healthy lungs: they are found in blood, not in lung tissue
- in an infected lung, they are recruited so good marker of inflammation
how can immune cells capture antigens?
- dendritic cells can extend their ‘arms’ across the epithelium and capture antigen from airway lumen
- M(icrofold) cells lining the epithelium take antigen from lumen to basal surface, where it is taken up by APCs
3 APCs
- dendritic cell (best)
- macrophage
- B lymphocyte
2 types of IgA
- serum IgA (IgA1 monomers) = pro-inflammatory (leads to phagocytosis, cytokines etc)
- secretory IgA (IgA2 dimers) = non-inflammatory = neutralisation of pathogens, toxins and antigens in lamina propria or airway lumen
how does secretory IgA move from the lamina propria to airway lumen
- made in lamina propria by plasma cells
- transported to mucosa via poly-Ig receptor
- poly-Ig receptor cleaves - the ‘secretory component’ remains attached to IgA and prevents secretory IgA from binding to Fca receptor on innate immune cells = non-inflammatory
why is secretory IgA non-inflammatory?
- b/c we want to be gentle to our own microflora since much of it is in the mucosa
how is all the mucosa in the body connected (immune-wise)?
- mucosal lymphocytes express their own homing receptors which are diff to other lymphocytes
- therefore they will circulate in mucosa all around the body
how do innate immune cells recognise pathogens?
- detect PAMPs and DAMPs (damage-associated) using pattern recognition receptors (PRRs)
- e.g. lipopolysaccharides in gram-negative bacteria
lineage of T cells
sensitisation (first step in allergy)
- allergen enters body and is phagocytosed (if skin > langerhans cell or if elsewhere, dendritic cells)
- presented to naïve Th cell on MHC II marker> TH2 cell secretes IL-4,5,13
- B cells differentiate into plasma cells > secrete IgE (class switching due to IL-4) which binds to mast cell and basophils by Fc region
allergic response (second step)
- upon secondary exposure to allergen, allergen binds to IgE on mast cells > crosslinks
- leads to degranulation and release of histamine > allergic response
- 2 phases: immediate reaction phase using existing chemical mediators (histamine) or late reaction phase using new chemical mediators (phospholipids, arachidonic acid, cytokines, prostaglandins)
pathological features of the asthmatic lung
- goblet cell hyperplasia > excessive mucus > wheezing
- remodelling of lung tissue = collagen deposition = less elasticity
- eosinophils = Th2 response
why is IgE involved in allergies?
- IgE evolved to protect from helminths and is essentially doing the same thing to allergens
allergen immunotherapy
- subcutaneous injection of allergen to induce immunological and physiological tolerance
- diverts Th2 response towards Treg and Th1
4 main lung lymph nodes
- pulmonary: angles of bifurcation of branching lobar bronchi
- bronchopulmonary (hilar)
- tracheobronchial: above/below bifurcation of trachea
- paratracheal: next to trachea