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Untitled - D Ank Unlimited

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Felton phenomenon 270 fetus allograft<br />

to BCG vaccine, but the delayed-type response is less<br />

intense than in other species. The granulomatous reaction<br />

to tuberculosis is essentially the same as in other mammals.<br />

The major histocompatibility complex (MHC) is<br />

designated FLA and is not polymorphic. The FLA system<br />

contains 10 to 20 class I gene loci, only two of which are<br />

expressed. They manifest five class II gene loci, only three<br />

of which are expressed. The lack of MHC polymorphism<br />

renders bone marrow transplantation very successful in this<br />

species. Cats possess all major complement components at<br />

levels equivalent to those in other mammals. The principal<br />

target organ for anaphylaxsis in the cat is the lung, where<br />

serotonin released from mast cells is the principal mediator.<br />

Flea bite dermatitis is the most frequent allergic skin<br />

disease of cats. Feline blood group antigens are designated<br />

A and B. In the United States, 99% of cats belong to group<br />

A and 1% to group B. Spontaneous autoimmune diseases in<br />

cats include hemolytic anemia, hyperthryoidism, thrombocytopenic<br />

purpura, pemphigus vulgaris, pemphigus foliaceous,<br />

myasthenia gravis, systemic lupus erythematosus,<br />

and arthritis. Cats only rarely have immunodeficiencies.<br />

Chediak–Higashi syndrome is the most common congenital<br />

defect in immune function. The leukocytes manifest<br />

large lysosomal granules, but susceptibility to infection is<br />

not increased. Colostral immunoglobulins are not passively<br />

transferred in cats. Secondary immunodeficiencies<br />

are attributable usually to feline leukemia virus (FeLV)<br />

infection, which often induces severe immunodeficiency in<br />

infected animals. Feline immunodeficiency virus (FIV) is a<br />

lentivirus that infects both domestic and wild cats. It leads<br />

to depletion of CD4 + T lymphocytes and resembles human<br />

AIDS. The virus receptor is mediated through fCD9 rather<br />

than fCD4. There is polyclonal stimulation of B cells and<br />

of fCD8 + T cells. The disease terminates in an AIDS-like<br />

condition. Cats also develop plasmacytomas, although they<br />

are not common.<br />

Felton phenomenon<br />

Specific immunologic unresponsiveness or paralysis<br />

induced by the inoculation of relatively large quantities of<br />

pneumococcal polysaccharide into mice.<br />

Felty’s syndrome<br />

A type of rheumatoid arthritis in which patients develop<br />

profound leukopenia and splenomegaly.<br />

feral mouse<br />

A mouse that returns to the wild from its former commensal<br />

existence.<br />

Fernandez reaction<br />

An early (24- to 48-hour) tuberculin-like delayed-type<br />

hypersensitivity reaction to lepromin observed in tuberculoid<br />

leprosy; a skin test for leprosy.<br />

ferritin<br />

An iron-containing protein that is electron dense and serves<br />

as a source of stored iron until it is needed for the synthesis<br />

of hemoglobulin. It is an excellent antigen and is found in<br />

abundant quantities in horse spleen. Ferritin’s electrondense<br />

quality makes it useful for labeling antibodies or for<br />

identifying and localizing antigens in electron microscopic<br />

preparations.<br />

ferritin labeling<br />

The conjugation of ferritin to antibody molecules to render<br />

them visible in histiologic or cytologic specimens observed<br />

by electron microscopy. Antibodies may be labeled with<br />

Red<br />

blood<br />

cell<br />

Ferritin-labeled<br />

antigen<br />

Receptor site<br />

Ferritin labeling.<br />

Visible on EM<br />

Not visible on EM<br />

ferritin by use of a crosslinking reagent such as toluene-2,4diisocyanate.<br />

The ferritin-labeled antibody may be reacted<br />

directly with the specimen, or ferritin-labeled antiimmunoglobulin<br />

may be used to react with unlabeled specific<br />

antibody attached to the target tissue antigen.<br />

fertilizin<br />

A glycoprotein present as a jelly-like substance surrounding<br />

sea urchin eggs. It behaves as an antigen-like substance<br />

from the standpoint of valence. Sperm, which contain<br />

proteinaceous antifertilizin, agglutinate into clumps when<br />

combined with soluble fertilizin, which is dissolved from<br />

eggs by acidified seawater.<br />

fetal antigen<br />

A fetal or oncofetal antigen expressed as a normal constituent<br />

of embryos and not in adult tissues. It is re-expressed in<br />

neoplasms of adult tissues, apparently as a result of derepression<br />

of the gene responsible for its formation.<br />

fetal–maternal tolerance<br />

Among mammals, a mother’s tolerance for her fetus that<br />

expresses allogeneic paternal MHC molecules. A fetus<br />

implanted into the uterus represents a tissue graft that<br />

avoids rejection. Its survival is facilitated by immune privilege<br />

and other factors.<br />

fetal thymic organ culture (FTC)<br />

The culture in vitro of thymic tissue excised from a fetal<br />

mouse. The thymus in culture retains the capacity to facilitate<br />

T lymphocyte development.<br />

fetus allograft<br />

Success of the haplo-nonidentical fetus as an allograft was<br />

suggested in the 1950s by Medawar, Brent, and Billingham<br />

to rely on four possibilities: (1) the conceptus might not<br />

be immunogenic, (2) pregnancy might alter the immune<br />

response, (3) the uterus might be an immunologically privileged<br />

site, and (4) the placenta might represent an effective<br />

immunological barrier between mother and fetus. Further<br />

studies have shown that transplantation privilege afforded<br />

the fetal–placental unit in pregnancy depends on intrauterine<br />

mechanisms. The pregnant uterus has been shown not to be<br />

an immunologically privileged site. Pregnancies usually are<br />

successful in maternal hosts with high levels of pre-existing<br />

alloimmunity. The temporary status has focused on specialized<br />

features of fetal trophoblastic cells that facilitate transplantation<br />

protection. Fetal trophoblast protects itself from<br />

maternal cytotoxic attack by failing to express on placental

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