INMUNOLOGÍA

1991

Artículos

Álvarez de Buergo M, García Consuegra J, Gómez Reino J, Gómez Reino JJ, Martínez Laso J, Cabello AA, Mateo I. Juvenile dermatomyositis: clinical and evolutive study. Acta Univ Carol Med (Praha). 1991;37(1-2):6-7.

Arnaiz Villena A, Pérez Aciego P, Ballestín C, Sotelo T, Pérez Seoane C, Martín Villa JM, et al. Biochemical basis of a novel T lymphocyte receptor immunodeficiency by immunohistochemistry. A possible CD3 gamma abnormality. Lab Invest. 1991;64(5):675-81.

Corell A, Martín Villa JM, Morales P, De Juan MD, Varela P, Vicario JL, et al. Exon-2 nucleotide sequences, polymorphism and haplotype distribution of a new HLA-DRB gene: HLA-DRB sigma. Mol Immunol. 1991;28(4-5):533-43.

Corell A, Martín Villa JM, Morales P, De Juan MD, Vicario JL, Martínez Laso J, et al. The HLA-DRB6 locus defines an evolutionary supratypic group within the DRB family of genes. Int J Cancer Suppl. 1991;6:26-9

Martín Villa JM, Regueiro JR, De Juan D, Pérez Aciego P, Pérez Blas M, Manzanares J, et al. T-lymphocyte dysfunctions occurring together with apical gut epithelial cell autoantibodies. Gastroenterology. 1991;101(2):390-7

Martínez Laso J, Vicario JL, Corell A, Martín Villa JM, Morales P, Lledó G, et al. Exclusive HLA-DQ factors do not explain susceptibility to insulin-dependent diabetes. Hum Immunol. 1991;31(2):134-8

Morales P, Martínez Laso J, Martín Villa JM, Corell A, Vicario JL, Varela P, et al. High frequency of the HLA-DRB1*0405-(Dw15)-DQw8 haplotype in Spaniards and its relationship to diabetes susceptibility. Hum Immunol. 1991;32(3):170-5

Pérez Aciego P, Alarcón B, Arnaiz Villena A, Terhorst C, Timón M, Segurado OG, et al. Expression and function of a variant T cell receptor complex lacking CD3-gamma. J Exp Med. 1991;174(2):319-26

Pérez Aciego P, Regueiro JR. Immunodeficiencies: Advanced in their caracterization and therapy. Inmunologia. 1991;10(1):10-14

Pérez Blas M, Arnaiz Villena A, Góngora R, Segurado OG, Vivanco JL, Regueiro JR. Impaired T cell signal transduction through CD28 in a patient with idiopathic thrombocytopenia. Clin Exp Immunol. 1991;85(3):424-8.

Postigo Llorente C, Ivars Amorós J, Ortiz de Frutos FJ, Regueiro JR, Llamas Martín R, Guerra Tapia A, et al. Cutaneous lesions in severe combined immunodeficiency: two case reports and a review of the literature. Pediatr Dermatol. 1991;8(4):314-21.

Segurado OG, Giles CM, Iglesias Casarrubios P, Corell A, Martínez Laso J, Vicario JL, et al. C4 Chido 3 and 6 distinguish two diabetogenic haplotypes: HLA-B49, SC01,DR4,DQw8 and B8,SC01,DR3,DQw2. Immunobiology. 1991;183(1-2):12-22

Segurado OG, Iglesias Casarrubios P, Martínez Laso J, Corell A, Martín Villa JM, Arnaiz Villena A. Autoimmunogenic HLA-DRB1*0301 allele (DR3) may be distinguished at the DRB1 non-coding regions of HLA-B8,DR3,Dw24 and B18,DR3,Dw25 haplotypes. Mol Immunol. 1991;28(1-2):189-92

Timón M, Arnaiz Villena A, Pérez Aciego P, Morales P, Benmamar D, Regueiro JR. A diallelic RFLP of the CD3-epsilon chain of the clonotypic T-lymphocyte receptor is not associated with certain autoimmune diseases. Hum Genet. 1991;86(4):363-4

Villa JMM, De Juan D, Villena AA. Informe sobre el IV taller nacional de autoinmunidad (Sevilla, 1990). Inmunologia. 1991;10(4):131-6

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1992

Artículos

Arnaiz Villena A, Timón M, Corell A, Pérez Aciego P, Martín Villa JM, Regueiro JR. Brief report: primary immunodeficiency caused by mutations in the gene encoding the CD3-gamma subunit of the T-lymphocyte receptor. N Engl J Med. 1992;327(8):529-33.

Arnaiz Villena A, Timón M, Rodríguez Gallego C, Pérez Blas M, Corell A, Martín Villa JM, et al. Human T-cell activation deficiencies. Immunol Today. 1992;13(7):259-65.

Corell A, Morales P, Varela P, Paz Artal E, Martín Villa JM, Martínez Laso J, et al. Allelic diversity at the primate major histocompatibility complex DRB6 locus. Immunogenetics. 1992;36(1):33-8. Erratum in: Immunogenetics. 1992;36(6):404-5

Luque I, Martín Villa JM, Arnaiz Villena A. Informe sobre el II simposio en inmunología. Autoinmunidad: aspectos básicos y clínicos (Friburgo, abril de 1992). Inmunologia. 1992;11(4):136-9

Martínez Laso J. Avances en el estudio genético de marcadores HAL en diversas etnias (Yokohama, 1991). Inmunologia. 1992;11(2):51-2

Ortiz Romero PL, López Estebaranz JL, Gil Martín R, Corell Almuzara A, Ballestín Carcavilla C, De Pablo Martín P, et al. Lymphomatoid papulosis: A study of 18 cases. J Eur Acad Dermatol Venereol. 1992;1(3):205-16

Pérez Blas M, Regueiro JR, Ruiz-Contreras JR, Arnaiz Villena A. T lymphocyte anergy during acute infectious mononucleosis is restricted to the clonotypic receptor activation pathway. Clin Exp Immunol. 1992;89(1):83-8.

Segurado OG, Arnaiz Villena AA, Iglesias Casarrubios P, Martínez Laso J, Vicario JL, Fontán G, et al. Combined total deficiency of C7 and C4B with systemic lupus erythematosus (SLE). Clin Exp Immunol. 1992;87(3):410-4.

Segurado OG, Iglesias Casarrubios P, Morales P, Martínez Laso J, Partanen J, Campbell RD, et al. Genetic structure of the novel low-frequency haplotype HLA-B49, SC01, DR4 and its contribution to insulin-dependent diabetes susceptibility. Immunogenetics. 1992;37(1):69-72.

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1993

Artículos

Arnaiz Villena A. MHC research: fast forward. Immunol Today. 1993;14(1):3-5.

Arnaiz Villena A, Timón M, Rodríguez Gallego C, Iglesias Casarrubios P, Pacheco A, Regueiro JR. T lymphocyte signalling defects and immunodeficiency due to the lack of CD3 gamma. Immunodeficiency. 1993;4(1-4):121-9.

Corell A, Varela P, Morales P, Paz Artal E, Martínez Laso J, Martín Villa JM, et al. A study of DR2-LUM haplotype generation and the DRB6*0202 linkage to DRB1*1601. Immunogenetics. 1993;38(6):460-1.

De Juan D, Martín Villa JM, Gómez Reino JJ, Vicario JL, Corell A, Martínez Laso J, et al. Differential contribution of C4 and HLA-DQ genes to systemic lupus erythematosus susceptibility. Hum Genet. 1993;91(6):579-84.

Martín Villa JM, De Juan D, Vicario JL, Luque IM, Álvarez E, Cortés Prieto J, et al. HLA class I, class II, and class III antigen sharing is not found in couples with unexplained infertility. Int J Fertil Menopausal Stud. 1993;38(5):280-8.

Morales P, Corell A, Martínez Laso J, Martín Villa JM, Varela P, Paz Artal E, et al. Three new HLA-G alleles and their linkage disequilibria with HLA-A. Immunogenetics. 1993;38(5):323-31.

Paz Artal E, Corell A, Varela P, Morales P, Martín Villa JM, Segurado OG,et al. New DNA sequences for the human complement gene C4. Mol Immunol. 1993;30(6):515-6.

Regueiro JR, Arnaiz Villena A, Vicario JL, Martínez Laso J, Pacheco A, Rivera Guzmán JM. A decrease in the estimated frequency of the extended HLA haplotype B18 CF130 DR3 DQw2 is common to non-insulin-dependent diabetes, juvenile rheumatoid arthritis, and Berger’s disease. Experientia. 1993;49(6-7):553-6.

Timón M, Arnaiz Villena A, Rodríguez Gallego C, Pérez Aciego P, Pacheco A, Regueiro JR. Selective disbalances of peripheral blood T lymphocyte subsets in human CD3 gamma deficiency. Eur J Immunol. 1993;23(7):1440-4.

Timón M, Arnaiz Villena A, Ruiz Contreras J, Ramos Amador JT, Pacheco A, Regueiro JR. Selective impairment of T lymphocyte activation through the T cell receptor/CD3 complex after cytomegalovirus infection. Clin Exp Immunol. 1993;94(1):38-42.

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1994

Artículos

Góngora R, Corell A, Regueiro JR, Carasol M, Rodríguez Gallego C, Paz Artal E, et al. Peripheral blood reduction of memory (CD29+, CD45RO+, and “bright” CD2+ and LFA-1+) T lymphocytes in Papillon-Lefèvre syndrome. Hum Immunol. 1994;41(3):185-92.

Martínez Laso J, Martín Villa JM, Álvarez M, Martínez Quiles N, Lledo G, Arnaiz-Villena A. Susceptibility to insulin-dependent diabetes mellitus and short cytoplasmic ATP-binding domain TAP2*01 alleles. Tissue Antigens. 1994;44(3):184-8.

Paz Artal E, Corell A, Álvarez M, Varela P, Allende L, Madroño A, et al. C4 gene polymorphism in primates: evolution, generation, and Chido and Rodgers antigenicity. Immunogenetics. 1994;40(6):381-96.

Rigopoulou D, Martínez Laso J, Martínez Tello F, Alcaide JF, Benmamar D, Hawkins F, et al. Both class I and class II HLA antigens are thyroid cancer susceptibility factors. Tissue Antigens. 1994;43(5):281-5.

Rodríguez Gallego C, Arnaiz Villena A, Corell A, Manzanares J, Timón M, Pacheco A, et al. Primary T lymphocyte immunodeficiency associated with a selective impairment of CD2, CD3, CD43 (but not CD28)-mediated signal transduction. Clin Exp Immunol. 1994;97(3):386-91.

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1995

Artículos

Arnaiz Villena A, Benmamar D, Álvarez M, Díaz Campos N, Varela P, Gómez Casado E, et al. HLA allele and haplotype frequencies in Algerians. Relatedness to Spaniards and Basques. Hum Immunol. 1995;43(4):259-68.

Arnaiz Villena A, Rodríguez Gallego C, Timón M, Corell A, Pacheco A, Álvarez Zapata D, et al. Diseases involving the T-cell receptor/CD3 complex. Crit Rev Oncol Hematol. 1995;19(2):131-47.

Martínez Laso J, De Juan D, Martínez Quiles N, Gómez Casado E, Cuadrado E, Arnaiz Villena A. The contribution of the HLA-A, -B, -C and -DR, -DQ DNA typing to the study of the origins of Spaniards and Basques. Tissue Antigens. 1995;45(4):237-45

Pablos JL, Carreira PE, Martín Villa JM, Montalvo G, Arnaiz Villena A, Gómez Reino JJ. Polymorphism of the heat-shock protein gene HSP70-2 in systemic lupus erythematosus. Br J Rheumatol. 1995;34(8):721-3

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1996

Artículos

Arnaiz Villena A, Martínez Laso J, Corell A, Allende L, Rosal M, Gómez Reino JJ,et al. Frequencies of HLA-A24 and HLA-DR4-DQ8 are increased and that of HLA-B blank is decreased in chronic toxic oil syndrome. Eur J Immunogenet. 1996 Jun;23(3):211-9 [doi

Corell A, Madroño A, Rodríguez C, Allende L, Arnaiz Villena A. Diagnóstico molecular de inmunodeficiencias primarias. Inmunologia. 1996;15(Supl 1):7-18

Sánchez-Izquierdo JA, Lumbreras C, Colina F, Martínez Laso J, Jiménez C, Gómez R, et al. Severe graft versus host disease following liver transplantation confirmed by PCR-HLA-B sequencing: report of a case and literature review. Hepatogastroenterology. 1996;43(10):1057-61

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1997

Artículos

Morales JM, Pascual Capdevila J, Campistol JM, Fernández Zatarain G, Muñoz MA, Andrés A, et al. Membranous glomerulonephritis associated with hepatitis C virus infection in renal transplant patients. Transplantation. 1997;63(11):1634-9

Ortiz Romero PL, Corell Almuzara A, López Estebaranz JL, Arranz FR, Ruiz Contreras J. Lupus like lesions in a patient with X-linked chronic granulomatous disease and recombinant X chromosome. Dermatology. 1997;195(3):280-3

Praga M, Paz Artal E, Hernández E, Segura J, Moreno MA, Morales JM, et al. Antiproteinuric effect of angiotensin-converting enzyme inhibition and C5b-9 urinary excretion in membranous glomerulonephritis. Nephrol Dial Transplant. 1997;12(12):2576-9

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1999

Artíoculos

Martín Villa JM, Corell A, Ramos Amador JT, Ruiz Contreras J, Arnaiz Villena A. Higher incidence of autoantibodies in X-linked chronic granulomatous disease carriers: random X-chromosome inactivation may be related to autoimmunity. Autoimmunity. 1999;31(4):261-4 [doi]

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2000

Artículos

Allende LM, García Pérez MA, Moreno A, Ruiz Contreras J, Arnaiz Villena A. Fourteen years’ follow-up of an autoimmune patient lacking the CD3 gamma subunit of the T-lymphocyte receptor. Blood. 2000;96(12):4007-8

Allende LM, Hernández M, Corell A, García Pérez MA, Varela P, Moreno A, et al. A novel CD18 genomic deletion in a patient with severe leucocyte adhesion deficiency: a possible CD2/lymphocyte function-associated antigen-1 functional association in humans. Immunology. 2000 Mar;99(3):440-50 [doi

Arnaiz Villena A, Vargas Alarcón G, Granados J, Gómez Casado E, Longas J, Gonzales Hevilla M, et al. HLA genes in Mexican Mazatecans, the peopling of the Americas and the uniqueness of Amerindians. Tissue Antigens. 2000;56(5):405-16 [doi]

Castro MJ, Morales P, Martínez Laso J, Allende L, Rojo Amigo R, González Hevilla M, et al. Evolution of MHC-G in humans and primates based on three new 3’UT polymorphisms. Hum Immunol. 2000;61(11):1157-63 [doi]

Castro MJ, Morales P, Martínez Laso J, Allende L, Rojo Amigo R, González Hevilla M, et al. Lack of MHC-G4 and soluble (G5, G6) isoforms in the higher primates, Pongidae. Hum Immunol. 2000;61(11):1164-8 [doi

Castro MJ, Morales P, Rojo Amigo R, Martínez Laso J, Allende L, Varela P, et al. Homozygous HLA-G*0105N healthy individuals indicate that membrane-anchored HLA-G1 molecule is not necessary for survival. Tissue Antigens. 2000;56(3):232-9 [doi]

Gómez Casado E, Del Moral P, Martínez Laso J, García Gómez A, Allende L, Silvera Redondo C, et al. HLA genes in Arabic-speaking Moroccans: close relatedness to Berbers and Iberians. Tissue Antigens. 2000;55(3):239-49 [doi]

Gómez Casado E, Martínez Laso J, González Hevilla M, Longas J, Rubio I, Silvera Redondo C, et al. A novel HLA-A*6816 allele possible generated by a point mutation in a Chilean from Punta Arenas (Magellan Strait). Immunogenetics. 2000;51(4-5):257-60 [doi]  

Paul P, Rouas-Freiss N, Moreau P, Cabestre FA, Menier C, Khalil-Daher I, et al. HLA-G, -E, -F preworkshop: tools and protocols for analysis of non-classical class I genes transcription and protein expression. Hum Immunol. 2000;61(11):1177-95 [doi]

Silvera Redondo C, Gómez Casado E, Martínez Laso J, Egea E, Garavito G, Varela P, et al. A new HLA-Cw allele (Cw*0808) found in a Colombian Mestizo individual possibly generated by an intralocus/interloci gene conversion. Immunogenetics. 2000;51(12):1053-7 [doi