Immuno 1, Assessing Immune Fxn Flashcards
What happens when the 3 major components (neuts, monos/MO, and complement) of the innate immune system don’t work or are deficient?
- Neutrophil dysfunction:
- recurrent, extracellular bacterial infections of skin, lungs, GI tract, and urinary tract - Monocyte/MO dysfunction:
- development of systemic fungal infections, intracellular bacterial infections, chronic viral infections - Complement deficiency:
- recurrent, extracellular bacterial infections of skin, lungs, GI tract, urinary tract
What happens when the 3 major components (B cells, CD4 T, CD8 T) of the adaptive immune system don’t work properly, due to dysfunction or decreased numbers of cells?
- CD4 T deficiency or dysfunction:
- recurrent and/or disseminated infections with protozoa, fungi, viruses, and intracellular bacteria - CD8 T deficiency or dysfunction:
- recurrent and/or disseminated viral, protozoal, and intracellular bacterial infections - B cell deficiency or dysfunction:
- recurrent, extracellular bacterial infections of skin, lungs, GI, urinary tract
What are the most common inherited immune deficiencies of animals?
Dogs, Cats, Equine, Bovine
- Dogs (rare)
- CVID (common variable immune deficiency); IgA deficiency - Cats (rare)
- Pelger-Huet anomaly’ Chediak Higashi syndrome - Equine
- SCID (severe combined immune deficiency); IgM - Bovine (rare)
- BLAD (bovine leukocyte adhesion deficiency)
What are the typical signs of inherited immune deficiencies?
- Early age of onset (before 1 yr)
- Recurrent or chronic bacterial infections
- Infections that don’t respond to standard therapy
- Unusual infections (e.g. atypical mycobacteria, disseminated Toxoplasma)
How commonly does acquired immune dysfunction in animals?
Dogs, cats, horses, cattle
Acquired immune dysfunction is very COMMON
Dogs: corticosteroid therapy; DM; Cushings
Cats: corticosteroid therapy; FeLV and FIV; FIP infection; DM
Equine: FPT; EIAV infection
Bovine: FPT; BVD infection
How can I use information from the CBC and SADP to assess immune function?
- Neuts and lymphs (high and low significant)
- cytologic appearance of lymphs and neuts
- # of monocytes (high is significant)
- globulin concentrations (mostly comprised of IgG)
After checking CBC, what is the next set of diagnostic tests for a patient with suspected immune deficiency?
- Measure serum immunoglobulin conc (IgG, IgA, IgM)
2. Quantitate the number of circulating T cells and B cells (flow cytometry)
What about more advanced immune function testing?
- measure complement concentrations
- assess neut and mono respiratory burst and phagocytosis
- assess lymphocyte cytokine production and proliferation
- assess neut and mono chemotaxis
If you diagnose inherited immune deficiency, is there anything you can do about it?
- Humoral immune deficiency (CVID; B cell deficiency)
- administer periodic plasma or WB transfusions
- administer hyperimmune globulin (e.g. high-titered parvo serum)
- aggressive, but short-term rotating program of antimicrobial therapy
- use probiotics or trans-faunation to displace pathogenic bacteria in the gut - Complement deficiency:
- administer fresh or fresh frozen plasma transfusion - CD4 T deficiency:
- administer non-specific immune stimulants to induce IFN-gamma production - CD8 T deficiency:
- administer immune stimulants to boost NK cell fxn (can substitute for CD8 cells)