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1.
Chromosomal organization of candidate genes involved in cholesterol gallstone formation: a murine gallstone map 总被引:33,自引:0,他引:33
Epidemiologic and family studies indicate that cholesterol gallstone formation is in part genetically determined. The major contribution to our current understanding of gallstone genes derives from animal studies, particularly cross-breeding experiments in inbred mouse strains that differ in genetic susceptibility to cholesterol gallstone formation (quantitative trait loci mapping). In this review we summarize how the combined use of genomic strategies and phenotypic studies in inbred mice has proven to be a powerful means of dissecting the complex pathophysiology of this common disease. We present a "gallstone map" for the mouse, consisting of all genetic loci that have been identified to confer gallstone susceptibility as well as putative candidate genes. Translation of the genetic loci and genes between mouse and human predicts chromosomal regions in the human genome that are likely to harbor gallstone genes. Both the number and the precise understanding of gallstone genes are expected to further increase with rapid progress of the genome projects, and multiple new targets for early diagnosis and prevention of gallstone disease should become possible. 相似文献
2.
Animal models of rheumatoid arthritis and related inflammation 总被引:3,自引:0,他引:3
The major, extensively studied, experimentally-induced rat and mouse models of arthritis with features resembling rheumatoid
arthritis are reviewed here. Etiopathogenetic studies that were recently published are emphasized. In summary, multiple triggering
stimuli can induce disease in genetically-prone strains of inbred rats and mice. Multiple genetic loci, including both MHC
and non-MHC, regulate disease expression in these animals. By comparison with other models of autoimmune disease, clustering
of regulatory loci within and among species is increasingly becoming evident. At the cellular level, both innate and acquired
immune systems are involved in the disease manifestations. At the molecular level, unbalanced chronic production of tumor
necrosis factor-a (TNF-a), interleukin (IL)-1, IL-6 and IL-12, as opposed to IL-4 and IL-10, is correlated with arthritis
disease susceptibility and severity. 相似文献
3.
Robert M. Plenge 《Current rheumatology reports》2009,11(5):351-356
Recent human genetic discoveries have increased our understanding of rheumatoid arthritis (RA) susceptibility. Genome-wide
association studies have expanded the number of validated RA risk loci beyond HLA-DRB1 “shared epitope” alleles to include
additional major histocompatibility complex (MHC) risk alleles and more than 10 regions outside the MHC. The newly discovered
risk alleles are common in the general population, have a modest effect on RA risk, and together explain less than 5% of the
variance in disease risk. Whereas the actual causal mutation and causal gene for most loci remain to be determined, these
studies are beginning to reveal general themes: many risk loci are associated with other autoimmune diseases; many genes fall
within discrete biological pathways (eg, the nuclear factor κ-light-chain-enhancer of activated B cells signaling pathway);
and human genetics can group diseases into clinically meaningful subset categories (eg, presence or absence of autoantibodies).
This review discusses recent RA genetic discoveries in terms of their potential to improve patient care. 相似文献
4.
Genetics and systemic lupus erythematosus 总被引:2,自引:0,他引:2
Systemic lupus erythematosus (SLE) is a complex, multifactorial autoimmune disease. Genetic factors are believed to contribute
to its pathogenesis. There have been numerous recent advances in the study of murine and human lupus genetics. In well-defined,
experimental, transgenic or gene-knockout mouse models, the development of lupus-like disease has implicated specific genes
and pathways in the disease pathogenesis. Linkage analyses have mapped multiple susceptibility loci and disease suppressive
loci using inbred strains of mice that spontaneously develop lupus-like disease. Elegant genetic dissection has demonstrated
that a component phenotype of SLE is displayed by each congenic strain carrying a single susceptibility locus on a resistant
genetic background, whereas polycongenic strains exhibit fatal lupus nephritis. These studies suggest that genes in separate
pathways can interact to augment or suppress the initiation and progression of systemic autoimmunity. In association studies
of human lupus, the contributions of the MHC loci, Fcg receptors, various cytokines, components of the complement cascade,
and proteins involved in apoptosis have been explored. Most recently, linkage analyses have been performed and provide many
chromosomal regions for further exploration for susceptibility genes. Studies to identify the genes in the susceptibility
regions are underway. An understanding of the genes involved in the development of lupus should provide targets for more focused
therapy in lupus. 相似文献
5.
Juvenile idiopathic arthritis (JIA), the most common cause of chronic arthritis in children, is believed to be influenced
by genetic factors. Recent studies on the genetics of JIA have not only validated proposed genetic associations but have also
led to the recognition of novel genetic associations. Studies of specific genes have been modeled on the premise of shared
autoimmunity, wherein genetic variants that predispose to other autoimmune phenotypes may also confer susceptibility to JIA.
The advent of genome-wide association studies has accelerated the detection of non-HLA susceptibility loci in other autoimmune
phenotypes and is likely to uncover novel JIA-associated variants as well. This review highlights recent genetic investigations
of JIA. 相似文献
6.
McIndoe RA Bohlman B Chi E Schuster E Lindhardt M Hood L 《Proceedings of the National Academy of Sciences of the United States of America》1999,96(5):2210-2214
One approach to understanding common human diseases is to determine the genetic defects responsible for similar diseases in animal models and place those defective genes in their corresponding biochemical pathways. Our laboratory is working with an animal model for human rheumatoid arthritis called collagen-induced arthritis (CIA). We are particularly interested in determining the location of disease-predisposing loci. To that end, we performed experiments to localize susceptibility loci for CIA in an F2 cross between the highly susceptible mouse strain DBA/1j and the highly resistant mouse strain SWR/j. Specifically, a quantitative trait locus analysis was performed to localize regions of the mouse genome responsible for susceptibility/severity to CIA. One susceptibility locus, Cia1 in the major histocompatibility locus, had been identified previously. Two additional loci were detected in our analysis that contribute to CIA severity (Cia2, Cia3) on chromosomes 2 and 6. A third locus was detected that contributes to the age of onset of the disease. This locus (Cia4) was located on chromosome 2 and was linked to the same region as Cia2. Determining the identity of these loci may provide insights into the etiology of human rheumatoid arthritis. 相似文献
7.
PURPOSE OF REVIEW: Pediatric arthritis is a heterogeneous group of chronic arthropathies that are influenced by complex genetic and perhaps environmental factors. Interacting genetic traits may one day be identified that provide the basis for predicting disease risk and other characteristics such as course, age of onset, and disease severity. The purpose of this review is to describe the recent progress towards identifying the multiple genes related to pediatric arthritis and understand how they relate to each other and to disease pathology. RECENT FINDINGS: Candidate gene studies are by far the most widely reported type of genetic studies to date for juvenile arthritis with only one genome-wide screen for juvenile rheumatoid/idiopathic arthritis published. Particular attention is paid to studies of candidate genes with potential immunological roles and those associated with other forms of autoimmunity. SUMMARY: Genomic studies may perhaps one day provide information to allow future classification systems of childhood arthritis to include molecular biomarkers as a complement to clinical observations, as well as understand how these genes or proteins relate to each other and to disease pathogenesis. 相似文献
8.
Large studies on the genetics of common rheumatic diseases, such as rheumatoid arthritis and systemic lupus erythematosus, have identified multiple polymorphisms related to disease susceptibility, including peptidylarginine deiminase 4 (PADI4) and protein tyrosine phosphatase N22 (PTPN22). Some of the identified genes are associated with multiple autoimmune disorders, and some seem to have unique associations with particular disease entities. Although the molecules encoded by these genes have a primary role in the molecular pathways of autoimmunity, genetic variations and contribution to disease susceptibility seem to vary between ethnic groups. In this Review, we report the findings on genes associated with rheumatoid arthritis and focus on the differences in the frequency of polymorphisms between various ethnic groups. 相似文献
9.
Clustering of non-major histocompatibility complex susceptibility candidate loci in human autoimmune diseases 总被引:18,自引:0,他引:18
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Kevin G. Becker Richard M. Simon Joan E. Bailey-Wilson Boris Freidlin William E. Biddison Henry F. McFarland Jeffrey M. Trent 《Proceedings of the National Academy of Sciences of the United States of America》1998,95(17):9979-9984
Human autoimmune diseases are thought to develop through a complex combination of genetic and environmental factors. Genome-wide linkage searches of autoimmune and inflammatory/immune disorders have identified a large number of non-major histocompatibility complex loci that collectively contribute to disease susceptibility. A comparison was made of the linkage results from 23 published autoimmune or immune-mediated disease genome-wide scans. Human diseases included multiple sclerosis, Crohn’s disease, familial psoriasis, asthma, and type-I diabetes (IDDM). Experimental animal disease studies included murine experimental autoimmune encephalomyelitis, rat inflammatory arthritis, rat and murine IDDM, histamine sensitization, immunity to exogenous antigens, and murine lupus (systemic lupus erythematosus; SLE). A majority (≈65%) of the human positive linkages map nonrandomly into 18 distinct clusters. Overlapping of susceptibility loci occurs between different human immune diseases and by comparing conserved regions with experimental autoimmune/immune disease models. This nonrandom clustering supports a hypothesis that, in some cases, clinically distinct autoimmune diseases may be controlled by a common set of susceptibility genes. 相似文献
10.
Rheumatoid factor revisited 总被引:3,自引:0,他引:3
PURPOSE OF REVIEW: Initial studies of the pathogenesis of rheumatoid arthritis focused on the role of rheumatoid factor and immune complex-associated vasculitis and synovitis. Subsequent work has delineated T cell responses, the role of cytokines, chemokines, and the aggressive nature of rheumatoid synovitis. Recent findings underscore the importance of humoral immunity in this entity and are the subject of this review. RECENT FINDINGS: By the discovery of anti-cyclic citrullinated peptide, anti-RA33, and anti-GPI antibodies in the human and mouse systems, respectively, the impact of humoral autoimmunity in rheumatoid arthritis regained remarkable interest. This review summarizes recent insights into humoral autoimmunity in rheumatoid arthritis in the context of the generation of rheumatoid factors, including B cell activation via toll-like receptors and genetic predispositions that can trigger the induction of rheumatoid arthritis. The generation of rheumatoid factors that can also be found during host defense against infectious agents and under pathologic conditions, such as rheumatoid arthritis, Sj?gren syndrome, and hepatitis C-associated mixed cryoglobulinemia after hepatitis C infection is likely the result of genetic predispositions and the intensity of the (primary) immune reaction. Models of the role of rheumatoid factors in health and disease, including related lymphomagenesis, will be discussed. SUMMARY: In patients with rheumatoid arthritis, the induction of rheumatoid factors can be taken as an indicator of severe disease with a striking involvement of B cell activation. Very recent clinical trials using B cell depletion support the concept that humoral immunity, as evidenced by the production of rheumatoid factors, plays a significant role in the course of the disease. 相似文献
11.
Human leukocyte antigen genes associated with rheumatoid arthritis are commonly found in the unaffected population, implying that causal mechanisms of disease involve interactions between these genes and other factors. A variety of approaches-genetic, structural, and immunologic-are used to explore possible molecular interactions that may contribute to understanding the basis for this disease association. The specific relation between human leukocyte antigen-DR4 alleles and rheumatoid arthritis remains one of the strongest and most thoroughly studied examples of human leukocyte antigen risk genes among human autoimmune disorders. 相似文献
12.
The common autoimmune endocrinopathies result from an interaction between environmental factors and genetic predisposition. Several chromosomal gene regions have been shown to contribute to more than one disease, supporting the clinical observation that the autoimmune endocrine diseases cluster within individuals and families. Genetic studies have implicated the major histocompatability complex (MHC)-human leucocyte antigen (HLA) genes on chromosome 6p21, although this chromosomal region does not explain all of the genetic contribution to the various disorders. Non-MHC-HLA genes, including disease-specific loci, are beginning to be identified and the publication of the draft sequence of the human genome will undoubtedly expediate future discoveries. Combined with the establishment of large cohorts of subjects with disease and the development of technology capable of performing high-throughput genotyping, genetic studies are likely to impact on the future treatment and prevention of the common autoimmune endocrine diseases. 相似文献
13.
Searching for the autoimmune thyroid disease susceptibility genes: from gene mapping to gene function 总被引:11,自引:0,他引:11
The autoimmune thyroid diseases (AITD) are complex diseases that are caused by an interaction between susceptibility genes and environmental triggers. Genetic susceptibility, in combination with external factors (e.g., dietary iodine), is believed to initiate the autoimmune response to thyroid antigens. Abundant epidemiological data, including family and twin studies, point to a strong genetic influence on the development of AITD. Various techniques have been used to identify the genes contributing to the etiology of AITD, including candidate gene analysis and whole genome screening. These studies have enabled the identification of several loci (genetic regions) that are linked with AITD, and in some of these loci putative AITD susceptibility genes have been identified. Some of these genes/loci are unique to Graves' disease (GD) and Hashimoto's thyroiditis (HT), and some are common to both diseases, indicating that there is a shared genetic susceptibility to GD and HT. The putative GD and HT susceptibility genes include both immune modifying genes (e.g., human leukocyte antigen, cytotoxic T lymphocyte antigen-4) and thyroid-specific genes (e.g., TSH receptor, thyroglobulin). Most likely these loci interact, and their interactions may influence disease phenotype and severity. It is hoped that in the near future additional AITD susceptibility genes will be identified and the mechanisms by which they induce AITD will be unraveled. 相似文献
14.
D McCurdy 《Current opinion in rheumatology》1999,11(5):399-407
Genes important in the connective tissue diseases are being recognized in two basic ways: association studies and linkage analysis. Traditionally, association studies have confirmed a genetic influence in disease pathogenesis, especially in systemic lupus erythematosus, rheumatoid arthritis, juvenile rheumatoid arthritis, and the spondyloarthropathies. One of the strongest associations is with the HLA region. As techniques improve, genome scan studies suggest that multiple genes are involved in each of the connective tissue diseases, with some genes in common that confer an autoimmune susceptibility. Linkage analysis is identifying new candidate genes that will help to explain the etiology of connective tissue diseases. 相似文献
15.
An update on genetic studies of systemic lupus erythematosus 总被引:8,自引:0,他引:8
Tsao BP 《Current rheumatology reports》2002,4(4):359-367
Systemic lupus erythematosus (SLE) is a complex, multifactorial autoimmune disease. Genetic factors are thought to contribute
to its pathogenesis. There have been numerous recent advances in the study of murine and human lupus genetics. In well-defined
experimental transgenic or gene-knockout mouse models, the development of lupus-like disease has implicated specific genes
and pathways in the disease pathogenesis. Linkage analyses have mapped multiple susceptibility loci and disease suppressive
loci using inbred strains of mice that spontaneously develop lupus-like disease. Elegant genetic dissection and function studies
have led to the recent identification of two murine candidate susceptibility genes, Ifi202 (encoding an interferon-inducible protein) and Cr2 (encoding complement receptors 1 and 2). In human lupus, casecontrol studies have established associations of SLE with certain
major histocompatibility class II alleles, complement deficiencies, and polymorphisms of Fcψ receptor genes, a complement-related
gene, and cytokine genes. During the past several years, linkage analyses using SLE multiplex families have provided many
chromosomal regions for further exploration of susceptibility genes. Six regions exhibiting significant linkage to SLE are
promising. Studies are underway to fine map these linked regions and to identify the genes in the susceptibility regions.
An understanding of the genes involved in the development of lupus should provide targets for more focused therapy in lupus. 相似文献
16.
Failure of distinction between self and non-self is regarded a critical event in the pathogenesis of several human diseases
such as systemic lupus erythematosus, rheumatoid arthritis, multiple sclerosis, myasthenia gravis, uveoretinitis or diabetes
mellitus. Autoagressive immune reactions driven by activated autoreactive lymphocytes are a characteristic feature of these
autoimmune diseases. The mechanisms by which the pathogenic control of autoreactive lymphocytes deviates from physiology can
be studied in appropriate animal models under well-defined experimental conditions. Experimental models of autoimmune diseases
in rodent inbred strains allow for the genetic mapping of susceptibility loci and might help to identify candidate genes also
relevant to the pathogenesis of human diseases. Finally, the experimental models are valuable tools to develop rational immunotherapeutic
strategies. Interesting features of some of the models employed for such research will be introduced in this review.
Received: 1 July 1997 / Accepted: 16 July 1997 相似文献
17.
There is convincing evidence to suggest a strong genetic component to psoriatic arthritis (PsA), with studies reporting a 40-fold risk to first-degree relatives of patients with disease. However, compared with rheumatoid arthritis, our understanding of the genetic etiology of PsA is less well-developed. Only three modestly sized genome-wide association studies of PsA have been undertaken to date, but they have identified the HLA-C region, IL12B, TRAF3IP2, and FBXL19 genes as being associated with PsA susceptibility. Results of genome-wide association studies of psoriasis and rheumatoid arthritis have been used to identify candidate genes for subsequent testing in PsA and have led to the identification of additional susceptibility factors for PsA. Most show overlap with psoriasis, whereas the overlap with rheumatoid arthritis is less pronounced. However, two loci show strong evidence for association with PsA but not psoriasis: HLA-B27 and the IL-13 gene locus. 相似文献
18.
Atherosclerosis is a complex and heritable disease involving multiple cell types and the interactions of many different molecular pathways. The genetic and molecular mechanisms of atherosclerosis have, in part, been elucidated by mouse models; at least 100 different genes have been shown to influence atherosclerosis in mice. Importantly, unbiased genome-wide association studies have recently identified a number of novel loci robustly associated with atherosclerotic coronary artery disease. Here, we review the genetic data elucidated from mouse models of atherosclerosis, as well as significant associations for human coronary artery disease. Furthermore, we discuss in greater detail some of these novel human coronary artery disease loci. The combination of mouse and human genetics has the potential to identify and validate novel genes that influence atherosclerosis, some of which may be candidates for new therapeutic approaches. 相似文献
19.
Previously, 4 children with deletion of the long arm of chromosome 18 and chronic arthritis were reported. We present an 8-year-old girl with arthritis, atrial septal defect, external auditory canal atresia, and developmental delay. She is the fifth child reported with 18q- syndrome and juvenile rheumatoid arthritis. Evidence is mounting that genetic loci on chromosome 18 may play a role in the expression of complex autoimmune diseases. Idiopathic arthritis should be considered as a potential additional feature in 18q- syndrome. 相似文献
20.
Holmdahl R 《Nature clinical practice. Rheumatology》2007,3(2):104-111
Complex traits, including inflammatory rheumatic diseases, have important genetic features, but most of the responsible genes have not been conclusively identified. Genetic analysis of inbred animal models and comparative genetics--the comparison of genes between different species--might help to identify the crucial genes and to investigate more directly the biology involved. Genome-wide linkage analysis of particular genes can be assessed by genetic segregation studies, whereas disease pathways can be delineated by the use of congenic strains. To clone disease genes, the traits need to be transformed so that they are inherited in a more Mendelian manner: achieving this pattern requires isolation of the locus on a genetic background that allows high penetrance by minimization of the size of congenic fragments, genetic manipulations without associated artifacts, or identification of highly penetrant mutations by phenotypic selection. Although almost one hundred quantitative trait loci for arthritis have been identified, only a few genes have so far been positionally cloned. In this Review we highlight the possibilities of using animal models to identify genes associated with complex diseases like arthritis, illustrated with available findings for genes such as those encoding major histocompatibility complex class II, neutrophil cytosolic factor 1 (Ncf1/p47(phox)) and ZAP70. 相似文献