Binds to the beta chain of TCR and MHC class II molecules of APC stimulating T cell activation
They are derived from large granular cells
Anti histone
Beta-pleated sheet, Hyaline globules
HIV affects CD4 cells.
Bloody diarrhea during infancy, low IgM and elevated IgA and IgE, large size platelets, atopic dermatitis.
CD45RO
Good cell mediated immunity
The most common polyarthritis condition in males is gout.
Antigen presentation and elimination
Cardiac tissue, Renal tissue, Splenic tissue, Hepatic tissue
Cytotoxic T cells
Congo red is the most specific stain for amyloid deposits.
The best method for confirming amyloidosis is a rectal biopsy.
2:1
It is present prior to antigenic exposure
Memory
Langerhans cell
Liver, Spleen, Kidney, Lung
Endothelial cells
CD4 T cell.
The best investigation for the diagnosis of amyloidosis is a rectal biopsy.
Monocyte Chemo-attractant Protein MCP-1
Present in nucleated cells
Periodic Acid Schiff (PAS) stain is specific for amyloid in tissue sections.
Kaposi’s sarcoma.
Wire loop lesions.
CNS
Amyloid associated protein, Mutant calcitonin, Mutant transthyretin, Normal transthyretin
Effective against virus infected cells
IgG
Macrophage
Rheumatoid arthritis
CD19
Graft must contain immunocompetent T cells
Sarcoidosis.
Syphilis.
Opsonisation.
Antibody production
Spleen
Type III
The treatment for asymptomatic HIV is done when CD4 count is below 350.
Complement component C3
IL-4
Skin
B cells
Rejection
Sickle Cell Disease
T-cells
Opportunistic infections
Both
Mucopolysaccharide, Lipoprotein, Glycoprotein
Acetylcholine receptors
Long arm of chromosome 6
IgG.
Organ transplant
Anti-double stranded DNA antibody.
MHC I
Toll-like receptor
A mechanism for the persistence and evolution of autoimmune disease is related to the immune response.
Killing of bacteria by helper cells
EBV (Epstein-Barr Virus) is associated with lymphoproliferative disorders.
Cells which express MHC1
Viral culture
MHC class I antigen
Cytotoxic T-lymphocyte mediated injury
Defect in the transport of chloride across epithelia.
Molecular mimicry
32
Anti RO
Type IV
Mature dendritic cell
Cardiac failure, Renal failure, Sepsis, Liver failure
Dark brown color, Blue color, Brilliant pink color, Khaki color
Presence of anti-donor antibodies
p24.
Sarcoidosis.
Decreased circulating lymphocytes
It is involved in anti-parasitic immune responses
Familial amyloidotic polyneuropathy, Dialysis associated amyloidosis, Prion protein associated amyloidosis
LE phenomenon, rheumatoid factor, anti-nuclear factor (ANF), double stranded DNA test.
Transient proteinuria.
Isograft, Allograft, Homograft, Xenograft
Systemic lupus erythematosus
IL-4
Alfa and Beta chain
Absent B cells
IgE
Primary CNS lymphoma
Acetylcholine receptors
ATTR amyloidosis is caused by mutations in transthyretin.
Anti-nuclear antibody.
Vascular graft failure is caused by endothelial cell dysfunction.
Present antigens for recognition by T cell antigen receptors
CD4 cell
Collection of monocytoid B – Cells in sinuses
Absent tonsils and no palpable lymph nodes on physical examination, female sex, high isohemagglutinins titers, low CD3.
Whole blood
Perforin and granzyme mediated apoptosis
CD 40 and CD 40L
AL amyloidosis is associated with renal failure.
Alpha and beta-1 chain
Monocyte
NK cells
Maturity onset DM, Type 1 DM, Type 2 DM, Equally seen with all forms of DM
Oral ulcers, psychosis, discoid rash, leucocytosis.
Hyperacute rejection
All of the above
Helps in the formation of antibody
All nucleated cells
Brain.
SLE.
Antigen Specific Receptors
Congo-red, Crystal violet, Methanamine silver
Common clinical manifestations of sarcoidosis include arthralgia, bilateral hilar adenopathy, erythema nodosum, and anterior uveitis.
Digeorge syndrome
Alzheimer’s disease, Chronic inflammatory states, Chronic renal failure, Malignant hypertension
Thymic hyperplasia
AA amyloidosis is associated with chronic inflammatory conditions.
Type II
Pneumonia, Chronic glomerulonephritis, Irritable bowel syndrome, Chronic osteomyelitis
Langerhan’s cells
Ankylosing spondylitis
All body cells
Mature dendritic cells