Skip to main content

Immunodeficiencies and Immunome: Diseases and Information Services

  • Chapter
  • First Online:
Clinical Applications of Immunomics

Part of the book series: Immunomics Reviews ((IMMUN,volume 2))

  • 545 Accesses

Abstract

Essential human immunome is composed of about 900 genes and proteins. Primary immunodeficiencies (IDs) are a large and heterogenic group of inherited disorders of the immune system. Since defects in any part of the adaptive or innate immune system can cause disorders, numerous IDs have been detected. Immunodeficiency patients have increased susceptibility to recurrent and persistent, even life-threatening infections. Other symptoms vary greatly between IDs. To date, some 200 IDs and 150 affected genes have been identified. ID-related genes are distributed throughout the genome. Features of IDs and information sources for them are discussed. Genotype–phenotype correlations are rather rare for IDs. Those diseases in which mutation type has effect on disease phenotype are described. ImmunoDeficiency Resource (IDR) is a comprehensive knowledge base for all essential information about IDs. The service is freely available at http://bioinf.uta.fi/IDR. IDdiagnostics (http://bioinf.uta.fi/IDdiagnostics) is dedicated to health professionals looking for laboratories performing gene and clinical tests for IDs. ID mutation data can be accessed in locus-specific, patient-related mutation databases, IDbases (http://bioinf.uta.fi/IDbases). Mutations are described at DNA, mRNA, and protein levels, with links to reference sequences and reference articles. The mutation data have been collated into entries, along with some clinical information. Currently, we have databases for 123 ID genes with 5359 patient entries. Immunome genes and proteins, their evolution, mouse–human comparisons, phylogenetics trees and orthologs for Metazoan immunome entities are available in Immunome Database, ImmTree, and ImmunomeBase all of which can be accessed via Immunome Knowledge Base (IKB) (http://bioinf.uta.fi/IKB).

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 129.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 169.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 169.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  • Ashburner, M., Ball, C. A., Blake, J. A., Botstein, D., Butler, H., Cherry, J. M., Davis, A. P., Dolinski, K., Dwight, S. S., Eppig, J. T., Harris, M. A., Hill, D. P., Issel-Tarver L., Kasarskis, A., Lewis, S., Matese, J. C., Richardson, J. E., Ringwald, M., Rubin, G. M., Sherlock, G. 2000. Gene ontology: tool for the unification of biology. The Gene Ontology Consortium. Nat. Genet. 25:25–29.

    CAS  Google Scholar 

  • Altschul, S. F., Madden, T. L., Schäffer, A. A., Zhang, J., Zhang, Z., Miller, W., Lipman, D. J. 1997. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res. 25:3389–3402.

    Article  PubMed  CAS  Google Scholar 

  • Antonarakis, S. E., Ashburner, M., Auerbach, A. D., Beaudet, A. L., Beckmann, J. S., Beutler, E., Cooper, D. N., Cotton, R. G. H., den Dunnen, J. T., Desnick, R. J., Eng, C., Fasman, K. H., Goldman, D., Hayashi, K., Hutchinson, F., Kazazian, H. H., Keen, J., King, M.-C., Lehväslaiho, H., McAlpine, P. J., McKusick, V., Motulski, A. G., Povey, S., Schorderet, D., Scriver, C. R., Shows, T. B., Superti-Furga, A., Tay, A. H. N., Tsui, L.-C., Valle, D., Vihinen, M. 1998. Recommendations for a nomenclature system for human gene mutations. Hum. Mut. 11: 1–3

    Article  PubMed  CAS  Google Scholar 

  • Arredondo-Vega, F. X., Santisteban, I., Daniels, S., Toutain, S., Hershfield, M. S. 1998. Adenosine deaminase deficiency: genotype-phenotype correlations based on expressed activity of 29 mutant alleles. Am. J. Hum. Genet. 63:1049–1059.

    Article  PubMed  CAS  Google Scholar 

  • Bonilla, F. A., Bernstein, I. L., Khan, D. A., Ballas, Z. K., Chinen, J., Frank, M. M., Kobrynski, L. J., Levinson, A. I., Mazer, B., Nelson, R. P. Jr., Orange, J. S., Routes, J. M., Shearer, W. T., Sorensen, R.U. 2005. Practice parameter for the diagnosis and management of primary immunodeficiency. Ann. Allergy Asthma Immunol. 94: S1–S63.

    Article  Google Scholar 

  • Bruford, E. A., Lush, M. J., Wright, M.W., Sneddon, T. P., Povey, S., Birney, E. 2008. The HGNC Database in 2008: a resource for the human genome. Nucleic Acids Res. 36:D445–448.

    Google Scholar 

  • Cavazzana-Calvo, M., Hacein-Bey, S., de Saint Basile, G., Gross, F., Yvon, E., Nusbaum, P., Selz, F., Hue, C., Certain, S., Casanova, J. L., Bousso, P., Deist, F. L., Fischer A. 2000. Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease. Science 288, 669–672.

    Article  PubMed  CAS  Google Scholar 

  • Castigli E, Wilson, S. A., Garibyan, L., Rachid, R., Bonilla, F., Schneider, L., Geha, R. S. 2005. TACI is mutant in common variable immunodeficiency and IgA deficiency. Nat. Genet. 37:829–834.

    Article  PubMed  CAS  Google Scholar 

  • Conley, M. E., Notarangelo, L. D., Etzioni, A. 1999. Diagnostic criteria for primary immunodeficiencies. Representing PAGID (Pan-American Group for Immunodeficiency) and ESID (European Society for Immunodeficiencies). Clin. Immunol. 93:190–197.

    CAS  Google Scholar 

  • Cotton, R. G. H., Auerbach, A. D., Beckmann J. S., Blumenfeld, O. O., Brookes, A. J., Brown, A. F., Carrera, P., Cox, D. W., Gottlieb, B., Greenblatt, M. S., Hilbert, P., Lehvaslaiho, H., Liang, P., Marsh, S., Nebert, D. W., Povey, A., Rossetti, S., Scriver, C. R., Summar, M., Tolan, D. R., Verma, I. C., Vihinen, M., den Dunnen, J. T. 2008. Recommendations for locus specific databases and their curation. Hum. Mut. 29:2–5.

    Google Scholar 

  • Dale, D. C., Person, R. E., Bolyard, A. A., Aprikyan, A. G., Bos, C., Bonilla, M. A., Boxer, L. A., Kannourakis, G., Zeidler, C., Welte, K., Benson, K. F., Horwitz, M. 2000. Mutations in the gene encoding neutrophil elastase in congenital and cyclic neutropenia. Blood 96:2317–2322.

    PubMed  CAS  Google Scholar 

  • den Dunnen, J. T., Antonarakis, S. E. 2000. Mutation nomenclature extensions and suggestions to describe complex mutations: A discussion. Hum. Mut. 15:7–12.

    Article  Google Scholar 

  • Eades-Perner, A. M., Gathmann, B., Knerr, V., Guzman, D., Veit, D., Kindle, G., Grimbacher, B. 2007. The European internet-based patient and research database for primary immunodeficiencies: results 2004–06. Clin Exp Immunol. 147:306–312.

    Article  PubMed  Google Scholar 

  • Fischer, A., Hacein-Bey, S., Cavazzana-Calvo, M. 2002. Gene therapy of severe combined immunodeficiencies. Nat. Rev. Immunol. 8:615–621.

    Google Scholar 

  • Giardine, B., Riemer, C., Hefferon, T., Thomas, D., Hsu, F., Zielenski, J., Sang, Y., Elnitski, L., Cutting, G., Trumbower, H., Kern, A., Kuhn, R., Patrinos, G. P., Hughes, J., Higgs, D., Chui, D., Scriver, C., Phommarinh, M., Patnaik, S. K., Blumenfeld, O., Gottlieb, B., Vihinen, M., Väliaho, J., Kent, J., Miller, W., Hardison, R. C. 2007. PhenCode: connecting ENCODE data with mutations and phenotype. Hum. Mut. 28:554–562.

    Article  PubMed  CAS  Google Scholar 

  • Hershfield, M.S. 2003. Genotype is an important determinant of phenotype in adenosine deaminase deficiency. Curr. Opin. Immunol. 15:571–577.

    Article  PubMed  CAS  Google Scholar 

  • Imai, K., Nonoyama, S., Ochs, H.D. 2003. WASP (Wiskott-Aldrich syndrome protein) gene mutations and phenotype. Curr. Opin. Allergy Clin. Immunol. 3:427–436.

    Article  PubMed  CAS  Google Scholar 

  • Infante, A. J., Britton, H. A., DeNapoli, T., Middelton, L. A., Lenardo, M. J., Jackson, C. E., Wang, J., Fleisher, T., Straus, S. E., Puck, J. M. 1998. The clinical spectrum in a large kindred with autoimmune lymphoproliferative syndrome caused by a Fas mutation that impairs lymphocyte apoptosis. J. Pediatr. 133:629–633.

    Article  PubMed  CAS  Google Scholar 

  • Johnston, J., Kelley, R. I., Feigenbaum, A., Cox, G. F., Iyer, G. S., Funanage, V. L., Proujansky, R. 1997. Am. J. Hum. Genet. 61:1053–1058.

    Article  CAS  Google Scholar 

  • Lindvall, J. M., Blomberg, K. E., Väliaho, J., Vargas, L., Heinonen, J. E., Berglof, A., Mohamed, A. J., Nore, B. F., Vihinen, M., Smith, C. I. E. 2005. Bruton's tyrosine kinase: cell biology, sequence conservation, mutation spectrum, siRNA modifications, and expression profiling. Immunol. Rev. 203:200–215.

    Article  PubMed  CAS  Google Scholar 

  • Lopéz-Granados, E., Pérez de Diego, R., Ferreira, Cerdán. A., Fontán, Casariego. G., García, Rodríguez. M. C. 2005. A genotype-phenotype correlation study in a group of 54 patients with X-linked agammaglobulinemia. J. Allergy Clin. Immunol. 116:690–697.

    Google Scholar 

  • Maródi, L., Notarangelo, L. D. 2007. Immunological and genetic bases of new primary immunodeficiencies. Nat. Rev. Immunol. 7:851–61.

    Article  PubMed  Google Scholar 

  • Notarangelo, L., Casanova, J. L., Fischer, A., Puck, J., Rosen, F., Seger, R., Geha, R. 2004. Primary immunodeficiency diseases: an update. J. Allergy Clin. Immunol. 114:677–687.

    Article  PubMed  CAS  Google Scholar 

  • Notarangelo, L. D., Hayward, A. R. 2000. X-linked immunodeficiency with hyper-IgM (XHIM). Clin. Exp. Immunol. 120:399–405.

    Article  PubMed  CAS  Google Scholar 

  • Notarangelo, L. D., Giliani, S., Mazza, C., Mella, P., Savoldi, G., Rodriguez-Pérez, C., Mazzolari, E., Duse, M., Plebani, A., Ugazio, A. G., Vihinen, M., Candotti, F., Schumacher, R. F. 2000. Of genes and phenotypes: The immunological spectrum of combined immune deficiency. Defects of the γc-JAK3 signaling pathway as a model. Immunol. Rev. 178:39–49.

    CAS  Google Scholar 

  • Ochs, H. H., Smith, C. I. E. and Puck, J. 2006. Primary immunodeficiency disaeses. A molecular and cellular approach. Oxford Univ. Press.

    Google Scholar 

  • Ortutay, C. and Vihinen, M. 2006. Immunome: a reference set for system biology on the human immune system. Cell. Immunol. 244:87–89.

    Google Scholar 

  • Ortutay, C., Siermala, M. and Vihinen, M. 2007a. Molecular characterization of the immune system: emergence of proteins, processes and domains. Immunogenet. 59:333–348.

    Google Scholar 

  • Ortutay, C., Siermala, M. and Vihinen, M. 2007b. ImmTree: database of evolutionary relationships of genes and proteins in the human immune system. Immunome Res. 3:4.

    Article  Google Scholar 

  • Piirilä, H., Väliaho, J. and Vihinen, M. 2006. Immunodeficiency mutation databases (IDbases). Hum. Mut. 27:1200–1208.

    Article  PubMed  Google Scholar 

  • Rannikko, K., Ortutay, C. and Vihinen, M. 2007. Immunity genes and their orthologs: a multi-species database. Int. Immunol. 19:1361–1370.

    Google Scholar 

  • Riikonen, P., Vihinen M. 1999. MUTbase: maintenance and analysis of distributed mutation databases. Bioinformatics 15:852–859.

    Article  PubMed  CAS  Google Scholar 

  • Salzer, U., Chapel, H. M., Webster, A. D., Pan-Hammarström, Q., Schmitt-Graeff, A., Schlesier, M., Peter, H. H., Rockstroh, J. K., Schneider, P., Schaffer, A. A., Hammarström, L., Grimbacher, B. 2005. Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans. Nat. Genet. 37:820–828.

    Article  PubMed  CAS  Google Scholar 

  • Samarghitean, C., Väliaho, J., Vihinen, M. 2004. Online registry of genetic and clinical immunodeficiency diagnostic laboratories, IDdiagnostics. J. Clin. Immunol. 24:53–61.

    Article  PubMed  Google Scholar 

  • Samarghitean, C., Väliaho, J., Vihinen, M. 2007. IDR knowledgebase for primary immunodeficiencies. Immunome Res. 3:6.

    Article  PubMed  Google Scholar 

  • Samarghitean, C. and Vihinen, M. 2008. Medical expert systems. Curr. Bioinf. 3:56–65.

    Google Scholar 

  • Scriver, C. R., Nowacki, P. M., Lehväslaiho, H. 1999. Guidelines and recommendations for content, structure and deployment of mutation databases. Hum. Mut. 13: 344–350.

    Article  PubMed  CAS  Google Scholar 

  • Väliaho, J., Riikonen, P., Vihinen, M. 2000. Novel immunodeficiency data servers. Immunol. Rev. 178:177–185.

    Article  PubMed  Google Scholar 

  • Väliaho, J., Pusa, M., Ylinen, T., Vihinen, M. 2002. IDR: the ImmunoDeficiency Resource. Nucleic Acids Res. 30:232–234.

    Article  PubMed  Google Scholar 

  • Väliaho, J., Riikonen, P., Vihinen, M. 2005. Distribution of immunodeficiency fact files with XML – from Web to WAP. BMC Med. Inform. Decis. Mak. 5:21.

    Article  PubMed  Google Scholar 

  • Väliaho, J., Smith, C. I. E., Vihinen, M. 2006. BTKbase: mutation database for X-linked agammaglobulinemia. Hum. Mut. 27:1209–1217.

    Article  PubMed  Google Scholar 

  • Verpy, E., Biasotto, M., Brai, M., Misiano, G., Meo, T., Tosi, M. 1996. Exhaustive mutation scanning by fluorescence-assisted mismatch analysis discloses new genotype-phenotype correlations in angiodema. Am. J. Hum. Genet. 59:308–319.

    PubMed  CAS  Google Scholar 

  • Vihinen, M., Vetrie, D., Maniar, H. S., Ochs, H. D., Zhu, Q., Vorechovský, I., Webster, A. D., Notarangelo, L. D., Nilsson, L., Sowadski, J. M., Smith, C. I. E. 1994. Structural basis for chromosome X-linked agammaglobulinemia: a tyrosine kinase disease. Proc. Natl. Acad. Sci. USA. 91:12803–12807.

    Article  PubMed  CAS  Google Scholar 

  • Vihinen, M., Cooper, M. D., de Saint Basile, G., Fischer, A., Good, R. A., Hendriks, R. W., Kinnon, C., Kwan, S. P., Litman, G. W., Notarangelo, L. D., Ochs, H. D., Rosen, F. S., Vetrie, D., Webster, A. D. B., Zegers, B. J. M, Smith, C. I. E. 1995. BTKbase: a database of XLA-causing mutations. Immunol. Today 16:460–465.

    Article  PubMed  CAS  Google Scholar 

  • Vihinen, M., Durandy, A. 2005. Primary immunodeficiencies: genotype-phenotype correlations. Immunogenomics and human disease (ed. Falus, A.) John Wiley and Sons. pp. 443–460.

    Google Scholar 

  • Vihinen, M., Kwan, S. P., Lester, T., Ochs, H. D., Resnick, I., Väliaho, J., Conley, M. E., Smith, C. I. E. 1999. Mutations of the human BTK gene coding for Bruton tyrosine kinase in X-linked agammaglobulinemia. Hum. Mutat. 13:280–285.

    Article  PubMed  CAS  Google Scholar 

  • Vihinen, M., Arredondo-Vega, F. X., Casanova, J. L., Etzioni, A., Giliani, S., Hammarström, L., Hershfield, M. S., Heyworth, P. G., Hsu, A. P., Lähdesmäki, A., Lappalainen, I., Notarangelo, L. D., Puck, J. M., Reith, W., Roos, D., Schumacher, R. F., Schwarz, K., Vezzoni, P., Villa, A., Väliaho, J., Smith, C. I. E. 2001. Primary immunodeficiency mutation databases. Adv. Genet. 43:103–188.

    Article  PubMed  CAS  Google Scholar 

  • Villa, A., Sobacchi, C., Notarangelo, L. D., Bozzi, F., Abinun, M., Abrahamsen, T. G., Arkwright, P. D., Baniyash, M., Brooks, E. G., Conley, M. E., Cortes, P., Duse, M., Fasth, A., Filipovich, A. M., Infante, A. J., Jones, A., Mazzolari, E., Muller, S. M., Pasic, S., Rechavi, G., Sacco, M. G., Santagata, S., Schroeder, M. L., Seger, R., Strina, D., Ugazio, A., Väliaho, J., Vihinen, M., Vogler, L. B., Ochs, H., Vezzoni, P., Friedrich, W., Schwarz, K. 2001. V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations. Blood 97:81–88.

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgments

Financial support from Finnish Academy and the Medical Research Fund of Tampere University Hospital is gratefully acknowledged.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Mauno Vihinen .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2009 Springer Science+Business Media, LLC

About this chapter

Cite this chapter

Vihinen, M. (2009). Immunodeficiencies and Immunome: Diseases and Information Services. In: Falus, A. (eds) Clinical Applications of Immunomics. Immunomics Reviews, vol 2. Springer, New York, NY. https://doi.org/10.1007/978-0-387-79208-8_4

Download citation

Publish with us

Policies and ethics