Monday, July 22, 2019

HLA-TYPING

AIDS
Ami
ATP
Aus
BAGE
BHRFI
BMLFI
BMRFI
BMT
BZLFI
c
CDK4
CDR
c.fes
CKS
CLIP
c.myc
COOH
c•pim
CREC
CSA.19
alanine
acquired immune deficiency syndrome
American Indian
antigen presenting cell
ankylosing spondylitis
adenosine triphosphate
Ausualian Aboriginal
beta-2 microglohulin
tumour antigen
Epstein-Barr virus lytic cycle antigen
Black
Epstein-Barr virus lytic cycle antigen
Epstein-Barr virus lytic cycle antigen
bone marrow transplantation
Epstein-Barr virus lytic cycle antigen
cysteine
congenital adrenal hyperplasia
cluster of differentiation
cell division control protein
cycline dependent kinase
complementarity determining region
proto-oncogene
cycline dependent kinase regulatory subunit
class II-associated invariant chain peptide
proto.oncogene
carboxy
proto-oncogene
cross-reacting group Of antigens
60S ribosomal protein LIOA

CDR
c-fes
c.myc
COOH
c•pim
CREC,
CSA-19
DDB'
DEK
Der p
EBNA
EBV
EMBL
ERP
ESAT
EST
complementarity determining region
to-oncogene
cycline dependent kinase regulatory subunit
class II-associated invariant chain peptide
carboxy
proto-oncogene
cross-reacting group of antigens
60S ribosomal protein L IOA
cytotoxic {or cytolytic' T lymphocyte
aspartic acid
DN A Bank Of 'apan
transcriptional regulatory protein
Derma tophagoides pteronyssinus
glutamic acid
Epstein •Barr virus nuclear antigen
Epstein-Barr virus
ethnic group
European Molecular Biology Laboratory
endoplasmic reticulum
endoplasmic reticulum resident protein
early secreted antigenic target 6 kDa protein
expressed sequence tag
Ets- I 
FcR 
C, 
GAD 
GAGE 
GBLP 
C.IcNac 
C,MCSF 
GSDB 
c,VHD 
C,VL 
HBV 
HCMV 
HCV 
HER.2/neu 
His 
HIV 
HPLC 
HPV 
HSI 
HSC 
HSP 
transcription factor 
phenylalanine 
ribosomal protein S30 fused to a ubiquitin-like 
Fe receptor 
glycme 
glutamic acid &carbOxylaSc 
tumour antigen 
guanine nucleotide binding protein b suburut•llke pre 
granulocyte / macrophage colony stimulating factot 
glycoprote.n 
melanoma anugen 'same as "melt 
Genome Seq ucnCC Database 
gait •versus•host disease 
graft •versus •leukemia 
hust idine 
histcxompatibility antigen 2 (of mice' 
hepatitis B virus 
human cytomegalovirus 
hepatitis C virus 
proto-oncogene 
Hispanic 
human immunodeficiency virus 
human leucocyte antigen 
high performance liquid chromatography 
human virus 
haematopoetic lineage cell specific protein 
heat protein constitutive 
heat protein 


HSC 
HSP 
Hsrn 
HSV' 
HTLV 
ICAM 
IDDM 
IFN 
IL 
Int-6 
rrAM 
ITIM 
kDa 
KIR 
heat shock protein constitutive 
heat shock protein 
human seminal 
herpes simplex Virus 
human T lymphotrophic Virus 
isoleucine 
intercellular adhesion molecule 
insuhn•dependent diabetes mellitis 
isoelectric focusing 
interferon 
immunoglobulin 
invariant cham 
interleukin 
immunoglobulin.like transcript 
translation imtiation factor subunit 
gamma interferon-inducible protein 
immuno•tyrosine activating motif 
immuno-tyrosine inhibitory motif 
lysine 
kilobase 
kilo-dalton 
killer.cell immunoglobulin.like receptor 
LOL 
LGL 
LIR 
Lmp 2/7 
Lmp• 112 
LOI p 
LRC 
M. 
MAGE 
MART.I/ 
MET 
MG 
MHC 
MIC 
Mix 
MLC 
MUWI 
NKC 
NMDP 
leucine 
low density lipoprotein 
large granular lymphocyte 
leukocyte immunoglobulin-like receptor 
low molecular mass polypeptides 2/7 
Epstein-Barr virus latent membrane protein 1/2 
lx»liurn perenne 
lymphocyte receptor complex 
methiomne 
Mycobacterium sp. 
melanoma anugen 
melanA / melanoma antigen 
megabase 
proto-oncogene 
myasthenia gravis 
major histocompaubility complex 
MHC class I •related chain 
MHC class II compartment 
mixed race 
mixed lymphocyte culture 
multiple sclerosis 
tumour antigen 
asparagine 
not available 
not determined 
natural killer 
natural killer complex 
United States National Marrow Donor Program 
NKC 
N',MDP 
Pac 
PCR 
PGK 
PLT 
pmel 
PRAME 
RAGE 
RBAP.2 
RFLP 
not determined 
natural killer 
natural killer complex 
Umted States National Marrow Donor Program 
nonstructural protein 
Oriental 
prohne 
Plasmodium sp. 
Pacific Islander 
rolymcrase chain reaction 
phosphoglycerate kinase 
primed lymphocyte typing 
melanoma antigen 
'Kilymerasc 
tumour antigen 
glutamine 
arginine 
rheumatoid arthritis 
tumour ant igen 
proto-oncogene 
retinoblastoma-associated protein 
restriction fragment length polymorphism 
sequence-based typing 
SHP 
SLE 
SMCY 
ssop 
ssp 
SSR 
ST ARP 
TAP 
TCR 
TIS 
TRAP 
TRP 
VLA 
SH2 domain containing protein 
systemic lupus erythematosis 
male.specific transplantation antigen 
sequence.specific oligonucleotide probe 
sequence-specific primer 
signal sequence receptor 
sporozoite threonine and asparagine rich protein 
threonine 
transporter associated with antigen processing 
HTLV•I trans activator 
receptor 
early response factor induced by growth and tumour promoters 
thrombospondin related anonymous protein 
melanoma antigen 
unknown amino acid 
valine 
adhesion receptor 
tryptophan 
isoleucine or leucine 


About a hundred years ago, biologists interested in cancer began to study the tumours that sometimes spontaneously arise in domesticated mice. Because each tumour died with the mouse in which it arose, investigators sought ways to transplant tumours from sick mice to healthy mice. In this way they hoped to prolong their investigations beyond the lifetime of a single mouse. In most of these experiments the transplanted tumour did not grow in the healthy recipient mouse, but was rejected by mechanisms that were later shown to be due to an immune response. However, when inbred stocks of mice were used, successful transplantation and propagation of tumours became feasible. The observations so made suggested that one or more genetic factors control the acceptance and rejection of tumour grafts. An important question to arise from these studies was whether the observed effects were restricted to tumours or also pertained to normal tissue. The latter was shown to be true: transplanted healthy tissues were subject to the same type of immunological rejection as transplanted tumours. Further study of the phenomenon was made possible by the generation of highly inbred strains of mice which to all intents and purposes were genetically homogeneous. Tissue transplants between mice Of the same inbred strain were shown to be accepted, whereas transplants between mice of different strains were always rejected. Breeding expenments made

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