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HLA type 337 homing<br />

Wells for different Ab<br />

+ lymphocytes + dye + complement<br />

polymerase chain reaction (PCR) methodology and DNA or<br />

oligonucleotide probes, especially for MHC class II typing.<br />

Class I typing involves reactions between lymphocytes to<br />

be typed with HLA antisera of known specificity in the<br />

presence of complement. Cell lysis is detected by phase or<br />

fluorescence microscopy. This is important in parentage<br />

testing, disease association, transfusion practices, and transplantation.<br />

HLA-A, -B, -C antigens should be defined by<br />

at least one of the following: (1) at least two different sera<br />

if both are monospecific, (2) one monospecific and two multispecific<br />

antisera, (3) at least three multispecific antisera<br />

if all multispecific types are used. Class II typing detects<br />

HLA-DR antigens using purified B cell preparations. It<br />

is based on antibody-specific, complement-dependent<br />

disruption of the membranes of lymphocytes. Cell death is<br />

demonstrated by the penetration of dye into the membrane.<br />

Class II typing is more difficult than type II methods and<br />

complement toxicity. At least three antisera must be used if<br />

all are monospecific, and at least five antisera must be used<br />

for multispecific sera.<br />

HLA type<br />

Both HLA class I and HLA class II allotypes expressed by<br />

an individual.<br />

HLA supertype<br />

Human MHC alleles with overlapping peptide-binding<br />

repertoires. The three HLA class I supertypes described<br />

include A2, A3, and B7.<br />

Hm-1<br />

Designation for the Syrian hamster major histocompatibility<br />

complex (MHC). MHC class II genes have been recognized.<br />

Hodgkin disease<br />

A type of lymphoma that involves the lymph nodes and<br />

spleen, causing a replacement of the lymph node architecture<br />

with binucleated giant cells known as Reed–Sternberg cells,<br />

reticular cells, neutrophils, eosinophils, and lymphocytes.<br />

Both lymphadenopathy and splenomegaly are present.<br />

Patients manifest deficiencies of cell-mediated immunity that<br />

cause tuberculin type skin tests to be negative. By contrast,<br />

their B cell functions are not altered. They may exhibit<br />

increases in suppressor cell activity and their susceptibility<br />

to opportunistic infections is increased. Antigen-presenting<br />

cells resembling dendritic cells apparently represent the<br />

transformed cell type. Hodgkin lymphoma, characterized by<br />

a predominance of lymphocytes, has a much better prognosis<br />

HLA tissue typing.<br />

Positive<br />

Dead<br />

cells<br />

Negative<br />

Live<br />

cells<br />

Hodgkin lymphoma; Hodgkin cell and Reed Sternberg cell.<br />

than does the nodular sclerosis variety of the disease in<br />

which the predominant cell type is nonlymphoid. Associated<br />

with transformed germinal center B cells.<br />

Hof<br />

German word for courtyard that refers to the perinuclear clear<br />

zone adjacent to the nuclei of plasma cells. Lymphoblasts and<br />

Reed–Sternberg cells may also exhibit hof zones.<br />

“hole in the repertoire” model<br />

A concept that proposes that an animal failing to respond<br />

to a given antigen is bereft of the requisite T cell specificity<br />

attributable to tolerance mechanisms. The relevant foreign<br />

peptide/self MHC combination is considered to closely<br />

resemble a self peptide/self MHC combination in the<br />

subject, leading to deletion of any T cell clones that would<br />

respond to the antigen as autoreactive during negative selection<br />

in the thymus or tolerization in the periphery. Thus, a<br />

“hole” exists in the individual’s T cell repertoire compared<br />

with the T cell repertoire of a responder.<br />

holoxenic<br />

An animal raised under ordinary conditions as opposed to<br />

an axenic or gnotobiotic animal.<br />

homeostasis<br />

In immunology, the maintenance of a constant and physiologic<br />

number of lymphocytes with a diverse repertoire even in<br />

the presence of new lymphocytes and exponential expansion<br />

of individual clones that follows immunogenic stimulation.<br />

homing<br />

The differential migration of lymphocytes or other leukocytes<br />

to specific tissues or organs.<br />

H

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