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Dive into the research topics where Cristina Campos is active.

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Featured researches published by Cristina Campos.


Open Medicine Journal | 2016

Ancestry of Amerindians and its Impact in Anthropology, Transplantation, HLA Pharmacogenomics and Epidemiology by HLA Study in Wiwa Colombian Population

A. Arnaiz-Villena; Ester Muñiz; Jose del Palacio-Gruber; Cristina Campos; Javier Alonso-Rubio; Eduardo Gomez-Casado; Filogonio Lopez-Pacheco; Manuel Martin-Villa; Carlos Silvera

RESEARCH ARTICLE Ancestry of Amerindians and its Impact in Anthropology, Transplantation, HLA Pharmacogenomics and Epidemiology by HLA Study in Wiwa Colombian Population Antonio Arnaiz-Villena, Ester Muñiz, Jose del Palacio-Gruber, Cristina Campos, Javier Alonso-Rubio, Eduardo Gomez-Casado, Filogonio Lopez-Pacheco, Manuel Martin-Villa and Carlos Silvera Department of Immunology, University Complutense, School of Medicine, Madrid Regional Blood Center, Madrid, Spain Department of Inmunología Animal, Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA), Autopista A6, Hipódromo, Madrid, Spain Department of Molecular Biology, Instituto Nacional de Cardiología Ignacio Chávez, Mexico City, Mexico Universidad del Norte, Barranquilla, Colombia


Human Immunology | 2016

Characterisation and functional implications of the two new HLA-G alleles found in Amerindian and Caribbean populations.

Antonio Arnaiz-Villena; Mercedes Enriquez-de-Salamanca; Jose Palacio-Gruber; Cristina Campos; Alejandro Camacho; José Manuel Martín-Villa; Narcisa Martinez-Quiles; Eduardo Gomez-Casado; Ester Muñiz

HLA-G polymorphism has been found to be relatively low in all world populations. In the present paper two new HLA-G molecules are described in ancient American natives. A new HLA-G molecule from a Ecuador Amerindian individual (male) showed four codon changes with respect to HLA-G*01:01:01. Silent changes at α1 domain (residue 57, Pro, CCG→CCA) and α2 domain (residue 93, His, CAC→CAT and residue 100, Gly, GGC→GGT) and one productive change in α3 domain (residue 219 changed from Arg to Trp). This α3 change may dramatically alter HLA-G interactions with beta-2 microglobulin, CD8, ILT-2 and ILT-4 ligands present in subsets of T, B, NK, monocytes, macrophages and dentritic cells. Another HLA-G new molecule was found in a woman from Hispaniola Island, Dominican Republic (Sto Domingo): it presented a silent change at α2 domain residue 107, Gly, GGA→GGT and non-silent change at residue 178, Met→Thr (with respect to HLA-G*01:01:01) which is close to class I molecule/clonotypic T cell receptor interaction sites. Functional implications of these findings are discussed.


PLOS ONE | 2017

Genetic HLA Study of Kurds in Iraq, Iran and Tbilisi (Caucasus, Georgia): Relatedness and Medical Implications.

Antonio Arnaiz-Villena; Jose Palacio-Gruber; Ester Muñiz; Cristina Campos; Javier Alonso-Rubio; Eduardo Gomez-Casado; Shadallah Fareq Salih; Manuel Martin-Villa; Rawand Al-Qadi; Tzen-Yuh Chiang

Kurds from Iraq (Dohuk and Erbil Area, North Iraq) have been analyzed for HLA genes. Their HLA genetic profile has been compared with that of other Kurd groups from Iran and Tbilisi (Georgia, Caucasus) and also Worldwide populations. A total of 7,746 HLA chromosomes have been used. Genetic distances, NJ dendrograms and correspondence analyses have been carried out. Haplotype HLA-B*52—DRB1*15 is present in all three analyzed Kurd populations. HLA-A*02-B*51-DRB1*11 is present in Iraq and Georgia Kurds. Haplotypes common to Iran and Iraq Kurds are HLA DRB1*11—DQB1*03, HLA DRB1*03—DQB1*02 and others in a lower frequency. Our HLA study conclusions are that Kurds most probably belong to an ancient Mediterranean / Middle East / Caucasian genetic substratum and that present results and those previously obtained by us in Kurds may be useful for Medicine in future Kurd transplantation programs, HLA Epidemiology (HLA linked diseases) and Pharmacogenomics (HLA-associated drug side effects) and also for Anthropology. It is discussed that one of the most ancient Kurd ancestor groups is in Hurrians (2,000 years BC).


Human Immunology | 2016

HLA-DMB in Amerindians: Specific linkage of DMB*01:03:01/DRB1 alleles

Antonio Arnaiz-Villena; Jose Palacio-Gruber; Ester Muñiz; Diego Rey; Maria J. Recio; Cristina Campos; Narcisa Martinez-Quiles; José Manuel Martín-Villa; Jorge Martinez-Laso

BACKGROUND HLA-DMB proteins are important for intracellular microbial metabolism in order other major histocompatibility complex (MHC) molecules present peptides to lymphocytes. In addition, HLA-DMB alleles have been found linked to diseases in some ethnic groups and HLA-DMB molecules may be important to explain HLA disease association. OBJECTIVE To detect HLA-DMB alleles profile in Amerindians for the first time and compare them to other populations. This will establish the bases to study HLA-DMB linkage to disease in Amerindians. METHOD A group of 168 voluntary Amerindians have been typed for HLA-DMB alleles. They have been characterized both, by genetic and genealogical bases. Cloning and automated HLA-DMB DNA (exons 2, 3 and 4) sequencing have been performed for allele assignation. RESULTS HLA-DMB*01:01:01 and HLA-DMB*01:03:01 show the highest frequencies. These have been compared to other World wide populations. HLA-DMB*01:03:01 is tightly associated to certain specific HLA-DRB1 alleles in Amerindians. CONCLUSION The specific Amerindian HLA-DMB allele frequencies and their linkage disequilibrium with other MHC alleles may be crucial to determine HLA-DMB World wide variation, evolution and specific linkage to disease in Amerindians and other populations.


Open Medicine Journal | 2018

HLA-G in Amerindians: Epidemiology and Worldwide Population Comparison

A. Arnaiz-Villena; Mercedes Enriquez-de-Salamanca; Jose Palacio-Gruber; Ignacio Juarez; Ester Muñiz; Jorge Nieto; Cristina Campos; Jose M. Martin-Villa

Received: November 9, 2017 Revised: December 23, 2017 Accepted: December 27, 2017 Abstract: Background: HLA-G molecules are immunosuppressive and avoid fetal rejection by giving negative signals to maternal immune system from fetal trophoblast cell surface. HLA-G genes have been associated to different pathologies: Spontaneous abortions, autoimmunity, tumor progression, transplant rejection and infection. In addition, different World populations show remarkable different HLA-G allele frequencies in the allele that does not produce a full HLA-G molecule (HLA-G*05N); this allele is almost absent in studied Amerindians.


Human Immunology | 2018

HLA in North Colombia Chimila Amerindians

Antonio Arnaiz-Villena; Jose Palacio-Gruber; Ignacio Juarez; Ennio Hernández; Ester Muñiz; Brayan Bayona; Cristina Campos; Jorge Nieto; Manuel Martin-Villa; Carlos Silvera

HLA-A,-B,-C,-DRB1 and -DQB1 alleles have been studied in Chimila Amerindians from Sabana de San Angel (North Colombian Coast) by using high resolution molecular typing. A frequent extended haplotype was found:HLA-A*24:02-B*51:10-C*15:02-BRB1*04:07-DQB1*03:02 (28.7%) which has also been described in Amerinndian Mayos Mexican population (Mexico, California Gulf, Pacific Ocean). Other haplotypes had already been found in Amerindians from Mexico (Pacific and Atlantic Coast), Peru (highlands and Amazon Basin), Bolivia and North USA. A geographic pattern according to HLA allele or haplotype frequencies is lacking in Amerindians, as already known. Also, five new extended haplotypes were found in Chimila Amerindians. Their HLA-A*24:02 high frequencies characteristic is shared with aboriginal populations of Taiwan; also, HLA-C*01:02 high frequencies are found in New Zealand Maoris, New Caledonians and Kimberly Aborigines from Australia. Finally, this study may show a model of evolutionary factors acting and rising one HLA allele frequency (-A*24:02), but not in others that belong to the same or different HLA loci.


Human Immunology | 2018

HLA Genes in Barranquilla (North Colombia): searching for cryptic Amerindian genes

Antonio Arnaiz-Villena; Brayan Bayona; Jose Palacio-Gruber; Ennio Hernández; Ester Muñiz; Cristina Campos; Ignacio Juarez; Eduardo Gomez-Casado; José Manuel Martín-Villa; Carlos Silvera

America First Inhabitants population (Amerindians, Na Dene and Eskimos) underwent a drastic population reduction and gene exchange after Europeans and Africans arrival after 1492 AD. Barranquilla population may be a good model to study present day population admixture in South America. HLA-A, -B and -DRB1 DNA typing has been performed in 188 unrelated individuals originated in the area and speak Spanish language; they showed apparent European/African and mixed characters. HLA genetic European/African features were found and only 1.85% Amerindian one. This contrasts with neighboring Cuban population where 10% HLA Amerindian characters appear.


The Open Ornithology Journal | 2017

Major Histocompatibility Complex Allele Persistence in Eurasia and America in the Genus During Million Years

Antonio Arnaiz-Villena; Valentin Ruiz-del-Valle; Ester Muñiz; Jose Palacio-Gruber; Cristina Campos; Eduardo Gomez-Casado; Jose Manuel Martín Villa; Ignacio Serrano-Vela

Genus Carduelis (Fringillidae family) includes goldfinches, siskins, redpolls, greenfinches and crossbills. Many of the species classified within this genus and other related genera have been grouped by using molecular systematics and the mitochondrial cytochrome b (mt cyt b) gene. According to this, the Eurasian siskin (C. spinus) is the only one extant direct ancestor of several North American finches; North American / South American radiations may have been originated by Eurasian siskin (or extinct relative). In the present work, we aim to perform a study of transpecies and transcontinental analyses of MHC (Major Histocompatibility Complex) Class I alleles in several genus Carduelis / Spinus species in order to draw evolutionary conclusions in several wild bird species belonging to the genus Carduelis / Spinus.


International Journal of Modern Anthropology | 2017

HLA genes in Atlantic Celtic populations: are Celts Iberians?

Antonio Arnaiz-Villena; Ana Carballo; Ignacio Juarez; Ester Muñiz; Cristina Campos; Beatriz Tejedor; Manuel Martin-Villa; Jose Palacio-Gruber

Atlantic Europe populations were analyzed with HLA genes in order to establish their relationship among themselves and with other populations. Standard genetic and statistical software analyses were used. Celtic populations (British Isles and French Bretons) have genetically been found close together: Irish, Welsh, Orkney Islanders (Scottish), French Bretons, Galicians, Spanish Basques, Portuguese, cluster together in DA genetic distances, correspondence analysis and Neighbour Joining dendrograms. Genetics have been shown by itself not suffice to determine populations migration/relatedness. Aristotle and Herodotus placed Celts in Iberia and R1b chromosome Y marker is high in Iberia and all Celtic European populations above mentioned (probably stemming from Iberian Ice refugee after Last Glaciation) and Ancient Celt language (Gaelic) is being translated from Iberian-Tartesian language: these suggest that Celts and Iberians, so named by Classic authors, constitute the same population. On the other hand, a) R1b gene analysis of Canary Islands ancient inhabitants (Guanches), b) abundant Iberian scripts are also found in Canary Islands, c) a established North Africa/Iberia ancient gene flow, and d) no evidence of demic diffusion from eastern to western Mediterranean according to human ancient skeleton studies is noticed in Mesolithic/Neolithic transition: these facts suggest that ancient Canary Islanders may be included within the Iberian/Celtic population. Our conclusions are that: 1) Celts are concentrated in Atlantic Europe, 2) Iberians and Celts mentioned by classic authors most probably refer to the same population living in Iberian Peninsula (Spain/Portugal); in addition, North African Berbers and ancient Canary Islanders also belong to this group 3) Postulated farmers demic diffusion in a East to West Mediterranean direction never existed. Keywords: Celts, Iberians, Picts, Scottish, Orkney Islands, Irish, British (English), French Bretons, Welsh, Basques, Galicians, Canary Islands, Mediterranean demic diffusion, Gaelic language


International Journal of Modern Anthropology | 2016

HLA genes in Chimila Amerindians (Colombia), the Peopling of America and Medical implications

Antonio Arnaiz-Villena; Jose Palacio-Gruber; Ester Muñiz; Cristina Campos; Javier Alonso-Rubio; Eduardo Gomez-Casado; David Cruz-Robles; Manuel Martin-Villa; Carlos Silvera

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Ester Muñiz

Gulf Coast Regional Blood Center

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Jose Palacio-Gruber

Gulf Coast Regional Blood Center

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Antonio Arnaiz-Villena

Gulf Coast Regional Blood Center

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Eduardo Gomez-Casado

Complutense University of Madrid

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Ignacio Juarez

Gulf Coast Regional Blood Center

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Manuel Martin-Villa

Complutense University of Madrid

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Narcisa Martinez-Quiles

Complutense University of Madrid

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Javier Alonso-Rubio

Gulf Coast Regional Blood Center

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Jorge Nieto

Gulf Coast Regional Blood Center

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