Skip to main content
Top
Published in: Journal of Clinical Immunology 2/2014

01-02-2014 | Original Research

Modeling Primary Immunodeficiency Disease Epidemiology and Its Treatment to Estimate Latent Therapeutic Demand for Immunoglobulin

Authors: Jeffrey S. Stonebraker, Albert Farrugia, Benjamin Gathmann, Jordan S. Orange, ESID Registry Working Party

Published in: Journal of Clinical Immunology | Issue 2/2014

Login to get access

Abstract

Purpose

Estimating the underlying demand for immunoglobulin (Ig) is important to ensure that adequate provision is made for patients with primary immune deficiency (PID) in the context of the competing demands for Ig and to ensure optimal therapeutic regimens. The concept of latent therapeutic demand (LTD) was used to estimate evidence-based requirements and compared to the actual Ig consumption in different countries. The estimates were performed for common variable immunodeficiency (CVID) and X-linked Agammaglobulinaemia (XLA), the two most commonly studied PIDs using Ig.

Methods

The LTD model for CVID and XLA was derived using decision analysis methodology. Data for the epidemiology and treatment variables were obtained from peer-reviewed publications, clinical registries and publicly-available patient surveys. Incomplete data records from registries were excluded from analysis. The variables impacting LTD were ranked in order of sensitivity through a tornado diagram. The uncertainty surrounding the variables was modeled using probabilistic distributions and evaluated using Monte Carlo simulation.

Results

Treatment dosage and prevalence were determined to be the most sensitive variables driving demand. The average potential usage of Ig for the treatment of CVID and XLA was estimated at 72 g per 1,000 population, which is higher than the estimated Ig usage in CVID and XLA of 27–41 g per 1,000 population in the US.

Conclusion

The potential demand for treating CVID and XLA exceeds the currently observed usage of Ig in these disorders. Variable usage in different countries is due to varying prevalence and dosage practices. Under-reporting in patient registries represents a major obstacle to calculating the true prevalence of CVID and XLA. Modeling demand relies heavily upon accurate prevalence and practice estimates which reemphasize the importance of accurate registries and improved registry methods. As better data becomes available, revision of model variables provides opportunities to anticipate and prepare for evolving patient needs.
Literature
1.
go back to reference Shehata N, Palda V, Bowen T, Haddad E, Issekutz TB, Mazer B, et al. The use of immunoglobulin therapy for patients with primary immune deficiency: an evidence-based practice guideline. Transfus Med Rev. 2010;24 Suppl 1:S28–50.PubMedCrossRef Shehata N, Palda V, Bowen T, Haddad E, Issekutz TB, Mazer B, et al. The use of immunoglobulin therapy for patients with primary immune deficiency: an evidence-based practice guideline. Transfus Med Rev. 2010;24 Suppl 1:S28–50.PubMedCrossRef
2.
3.
go back to reference Eibl MM. History of immunoglobulin replacement. Immunol Allergy Clin N Am. 2008;28(4):737–64.CrossRef Eibl MM. History of immunoglobulin replacement. Immunol Allergy Clin N Am. 2008;28(4):737–64.CrossRef
4.
go back to reference Hooper JA. Intravenous immunoglobulins: evolution of commercial IVIG preparations. Immunol Allergy Clin N Am. 2008;28(4):765–78.CrossRef Hooper JA. Intravenous immunoglobulins: evolution of commercial IVIG preparations. Immunol Allergy Clin N Am. 2008;28(4):765–78.CrossRef
5.
go back to reference Buchacher A, Iberer G. Purification of intravenous immunoglobulin G from human plasma—aspects of yield and virus safety. Biotechnol J. 2006;1(2):148–63.PubMedCrossRef Buchacher A, Iberer G. Purification of intravenous immunoglobulin G from human plasma—aspects of yield and virus safety. Biotechnol J. 2006;1(2):148–63.PubMedCrossRef
8.
go back to reference Orange JS, Hossny EM, Weiler CR, Ballow M, Berger M, Bonilla FA, et al. Use of intravenous immunoglobulin in human disease: a review of evidence by members of the primary immunodeficiency committee of the American academy of allergy, asthma and immunology. J Allergy Clin Immunol. 2006;117(4 Suppl):S525–53.PubMedCrossRef Orange JS, Hossny EM, Weiler CR, Ballow M, Berger M, Bonilla FA, et al. Use of intravenous immunoglobulin in human disease: a review of evidence by members of the primary immunodeficiency committee of the American academy of allergy, asthma and immunology. J Allergy Clin Immunol. 2006;117(4 Suppl):S525–53.PubMedCrossRef
11.
go back to reference Farrugia A, Cassar J. Is self-sufficiency in haemotherapies a practical or necessary goal? Blood Transfus. 2012;13:1–12. Farrugia A, Cassar J. Is self-sufficiency in haemotherapies a practical or necessary goal? Blood Transfus. 2012;13:1–12.
12.
go back to reference Rossi F, Perry R, de Wit J, Evers T, Folléa G. How expanding voluntary non-remunerated blood donations would benefit patients, donors and healthcare systems? Vox Sang. 2011;101(2):176–7.PubMedCrossRef Rossi F, Perry R, de Wit J, Evers T, Folléa G. How expanding voluntary non-remunerated blood donations would benefit patients, donors and healthcare systems? Vox Sang. 2011;101(2):176–7.PubMedCrossRef
13.
go back to reference Joshi AY, Iyer VN, Hagan JB, St Sauver JL, Boyce TG. Incidence and temporal trends of primary immunodeficiency: a population-based cohort study. Mayo Clin Proc. 2009;84(1):16–22.PubMedCentralPubMedCrossRef Joshi AY, Iyer VN, Hagan JB, St Sauver JL, Boyce TG. Incidence and temporal trends of primary immunodeficiency: a population-based cohort study. Mayo Clin Proc. 2009;84(1):16–22.PubMedCentralPubMedCrossRef
14.
go back to reference Orange JS, Grossman WJ, Navickis RJ, Wilkes MM. Impact of trough IgG on pneumonia incidence in primary immunodeficiency: a meta-analysis of clinical studies. Clin Immunol. 2010;137(1):21–30.PubMedCrossRef Orange JS, Grossman WJ, Navickis RJ, Wilkes MM. Impact of trough IgG on pneumonia incidence in primary immunodeficiency: a meta-analysis of clinical studies. Clin Immunol. 2010;137(1):21–30.PubMedCrossRef
15.
go back to reference Goel V. Decision analysis: applications and limitations. The Health Services Research Group. CMAJ. 1992;147(4):413–7.PubMedCentralPubMed Goel V. Decision analysis: applications and limitations. The Health Services Research Group. CMAJ. 1992;147(4):413–7.PubMedCentralPubMed
16.
go back to reference Stonebraker JS, Amand RE, Bauman MV, Nagle AJ, Larson PJ. Modelling haemophilia epidemiology and treatment modalities to estimate the unconstrained factor VIII demand. Haemophilia. 2004;10(1):18–26.PubMedCrossRef Stonebraker JS, Amand RE, Bauman MV, Nagle AJ, Larson PJ. Modelling haemophilia epidemiology and treatment modalities to estimate the unconstrained factor VIII demand. Haemophilia. 2004;10(1):18–26.PubMedCrossRef
17.
go back to reference Stonebraker JS, Keefer DL. Modeling potential demand for supply-constrained drugs: a new hemophilia drug at Bayer Biological Products. Oper Res. 2009;57(1):19–31.CrossRef Stonebraker JS, Keefer DL. Modeling potential demand for supply-constrained drugs: a new hemophilia drug at Bayer Biological Products. Oper Res. 2009;57(1):19–31.CrossRef
19.
go back to reference Gathmann B, Grimbacher B, Beauté J, Dudoit Y, Mahlauoui N, Fischer A, et al. The European internet-based patient and research database for primary immunodeficiencies: results 2006–2008. Clin Exp Immunol. 2009;157 Suppl 1:3–11.PubMedCentralPubMedCrossRef Gathmann B, Grimbacher B, Beauté J, Dudoit Y, Mahlauoui N, Fischer A, et al. The European internet-based patient and research database for primary immunodeficiencies: results 2006–2008. Clin Exp Immunol. 2009;157 Suppl 1:3–11.PubMedCentralPubMedCrossRef
20.
go back to reference Immune Deficiency Foundation: Primary immune deficiency diseases in America. Prepared by Schulman, Ronca and Bucuvalas, Inc., 1995. Immune Deficiency Foundation: Primary immune deficiency diseases in America. Prepared by Schulman, Ronca and Bucuvalas, Inc., 1995.
21.
go back to reference Immune Deficiency Foundation: Primary immune deficiency diseases in America: 2002. The second national survey of patients. Prepared by Schulman, Ronca and Bucuvalas, Inc., April 28, 2003 Immune Deficiency Foundation: Primary immune deficiency diseases in America: 2002. The second national survey of patients. Prepared by Schulman, Ronca and Bucuvalas, Inc., April 28, 2003
22.
go back to reference Immune Deficiency Foundation: Treatment experiences and preferences of patients with primary immune deficiency diseases: First national survey. Prepared by Schulman, Ronca and Bucuvalas, Inc., June 20, 2003. Immune Deficiency Foundation: Treatment experiences and preferences of patients with primary immune deficiency diseases: First national survey. Prepared by Schulman, Ronca and Bucuvalas, Inc., June 20, 2003.
23.
go back to reference Immune Deficiency Foundation: Primary immunodeficiency diseases in America: 2007. The third national survey of patients. Prepared by Abt SRBI, Inc., May 1, 2009. Immune Deficiency Foundation: Primary immunodeficiency diseases in America: 2007. The third national survey of patients. Prepared by Abt SRBI, Inc., May 1, 2009.
24.
go back to reference Immune Deficiency Foundation: Treatment experiences and preferences among patients with primary immunodeficiency diseases. National survey of patients: 2008. Prepared by Abt, SRBI, Inc., May 6, 2009. Immune Deficiency Foundation: Treatment experiences and preferences among patients with primary immunodeficiency diseases. National survey of patients: 2008. Prepared by Abt, SRBI, Inc., May 6, 2009.
25.
go back to reference Briggs AH, Weinstein MC, Fenwick EAL, Karnon J, Sculpher MJ, Paltiel AD, et al. Model parameter estimation and uncertainty analysis: a report of the ISPOR-SMDM modeling good research practices task force working group—6. Med Decis Mak. 2012;32:722–32.CrossRef Briggs AH, Weinstein MC, Fenwick EAL, Karnon J, Sculpher MJ, Paltiel AD, et al. Model parameter estimation and uncertainty analysis: a report of the ISPOR-SMDM modeling good research practices task force working group—6. Med Decis Mak. 2012;32:722–32.CrossRef
26.
go back to reference Keefer DL, Bodily SE. Three-point approximation for continuous random variables. Manag Sci. 1983;29:595–609.CrossRef Keefer DL, Bodily SE. Three-point approximation for continuous random variables. Manag Sci. 1983;29:595–609.CrossRef
27.
go back to reference Park MA, Li JT, Hagan JB, Maddox DE, Abraham RS. Common variable immunodeficiency: a new look at an old disease. Lancet. 2008;372(9637):489–502.PubMedCrossRef Park MA, Li JT, Hagan JB, Maddox DE, Abraham RS. Common variable immunodeficiency: a new look at an old disease. Lancet. 2008;372(9637):489–502.PubMedCrossRef
28.
go back to reference Yong PFK, Tarzi M, Chua I, Grimbacher B, Chee R. Common variable immunodeficiency: an update on etiology and management. Immunol Allergy Clin N Am. 2008;28(2):367–86.CrossRef Yong PFK, Tarzi M, Chua I, Grimbacher B, Chee R. Common variable immunodeficiency: an update on etiology and management. Immunol Allergy Clin N Am. 2008;28(2):367–86.CrossRef
30.
go back to reference Abuzakouk M, Feighery C. Primary immunodeficiency disorders in the Republic of Ireland: first report of the National Registry in children and adults. J Clin Immunol. 2005;25(1):73–7.PubMedCrossRef Abuzakouk M, Feighery C. Primary immunodeficiency disorders in the Republic of Ireland: first report of the National Registry in children and adults. J Clin Immunol. 2005;25(1):73–7.PubMedCrossRef
31.
go back to reference Beauté J et al. The French national registry of primary immunodeficiency diseases. Clin Immunol. 2010;135:264–72.CrossRef Beauté J et al. The French national registry of primary immunodeficiency diseases. Clin Immunol. 2010;135:264–72.CrossRef
32.
go back to reference Boyle JM, Buckley RH. Population prevalence of diagnosed primary immunodeficiency diseases in the United States. J Clin Immunol. 2007;27:497–502.PubMedCrossRef Boyle JM, Buckley RH. Population prevalence of diagnosed primary immunodeficiency diseases in the United States. J Clin Immunol. 2007;27:497–502.PubMedCrossRef
33.
go back to reference Edgar JDM, Buckland M, Guzman D, Conlon NP, Knerr V, et al. The United Kingdom Primary Immune Deficiency (UKPID) Registry: report of the first 4 years’ activity 2008–2012. Clin Exp Immunol doi: 10.1111/cei.12172. Edgar JDM, Buckland M, Guzman D, Conlon NP, Knerr V, et al. The United Kingdom Primary Immune Deficiency (UKPID) Registry: report of the first 4 years’ activity 2008–2012. Clin Exp Immunol doi: 10.​1111/​cei.​12172.
34.
go back to reference Gathmann B, Goldacker S, Klima M, et al. The German national registry for primary immunodeficiencies (PID). Clin Exp Immunol. 2013;173(2):372–80.PubMedCrossRef Gathmann B, Goldacker S, Klima M, et al. The German national registry for primary immunodeficiencies (PID). Clin Exp Immunol. 2013;173(2):372–80.PubMedCrossRef
35.
go back to reference Golan H et al. The incidence of primary immunodeficiency syndromes in Israel. IMAJ. 2002;4(Suppl):868–71.PubMed Golan H et al. The incidence of primary immunodeficiency syndromes in Israel. IMAJ. 2002;4(Suppl):868–71.PubMed
36.
go back to reference Ishimura M et al. Nationwide survey of patients with primary immunodeficiency diseases in Japan. J Clin Immunol. 2011;31:968–76.PubMedCrossRef Ishimura M et al. Nationwide survey of patients with primary immunodeficiency diseases in Japan. J Clin Immunol. 2011;31:968–76.PubMedCrossRef
37.
go back to reference Kirkpatrick P, Riminton S. Primary immunodeficiency diseases in Australia and New Zealand. J Clin Immunol. 2007;27(5):517–24.PubMedCrossRef Kirkpatrick P, Riminton S. Primary immunodeficiency diseases in Australia and New Zealand. J Clin Immunol. 2007;27(5):517–24.PubMedCrossRef
38.
go back to reference Flori NM, Llambi JM, Boren TE, Borja SR, Casariego GF. Primary immunodeficiency syndrome in Spain: first report of the National Registry in children and adults. J Clin Immunol. 1997;17(4):333–9.CrossRef Flori NM, Llambi JM, Boren TE, Borja SR, Casariego GF. Primary immunodeficiency syndrome in Spain: first report of the National Registry in children and adults. J Clin Immunol. 1997;17(4):333–9.CrossRef
39.
go back to reference Modell V, Gee B, Lewis DB, Orange JS, Rolfman CM, Routes JM, et al. Global study of primary immunodeficiency diseases (PI)—diagnosis, treatment, and economic impact: an updated report from the Jeffrey Modell Foundation. Immunol Res. 2011;51:61–70.PubMedCrossRef Modell V, Gee B, Lewis DB, Orange JS, Rolfman CM, Routes JM, et al. Global study of primary immunodeficiency diseases (PI)—diagnosis, treatment, and economic impact: an updated report from the Jeffrey Modell Foundation. Immunol Res. 2011;51:61–70.PubMedCrossRef
40.
go back to reference Resnick ES, Bhatt P, Sidi P, Cunningham-Rundles C. Examining the use of ICD-9 Diagnosis Codes for primary immune deficiency diseases in New York State. J Clin Immunol. 2013;33:40–8.PubMedCentralPubMedCrossRef Resnick ES, Bhatt P, Sidi P, Cunningham-Rundles C. Examining the use of ICD-9 Diagnosis Codes for primary immune deficiency diseases in New York State. J Clin Immunol. 2013;33:40–8.PubMedCentralPubMedCrossRef
41.
go back to reference Ryser O, Morell A, Hitzig WH. Primary immunodeficiencies in Switzerland: first report of the National Registry in adults and children. J Clin Immunol. 1988;8(6):479–85.PubMedCrossRef Ryser O, Morell A, Hitzig WH. Primary immunodeficiencies in Switzerland: first report of the National Registry in adults and children. J Clin Immunol. 1988;8(6):479–85.PubMedCrossRef
42.
go back to reference Stray-Pedersen A, Abrahamsen TG, Frøland SS. Primary immunodeficiency diseases in Norway. J Clin Immunol. 2000;20(6):477–85.PubMedCrossRef Stray-Pedersen A, Abrahamsen TG, Frøland SS. Primary immunodeficiency diseases in Norway. J Clin Immunol. 2000;20(6):477–85.PubMedCrossRef
43.
go back to reference Furst DE. Serum immunoglobulins and risk of infection: how long can you go? Semin Arthritis Rheum. 2009;39(1):18–29.PubMedCrossRef Furst DE. Serum immunoglobulins and risk of infection: how long can you go? Semin Arthritis Rheum. 2009;39(1):18–29.PubMedCrossRef
44.
go back to reference McDowell MA, Fryar CD, Ogden CL, Flegal KM. Anthropometric reference data for children and adults: United States, 2003–2006. National Health Statistics Reports: no. 10. Hyattsville: National Center for Health Statistics; 2008. McDowell MA, Fryar CD, Ogden CL, Flegal KM. Anthropometric reference data for children and adults: United States, 2003–2006. National Health Statistics Reports: no. 10. Hyattsville: National Center for Health Statistics; 2008.
45.
go back to reference Klein RJ, Schoenborn CA. Age adjustment using the 2000 projected U.S. population. Healthy People Statistics notes, no. 20. Hyattsville: National Center for Health Statistics; 2001. Klein RJ, Schoenborn CA. Age adjustment using the 2000 projected U.S. population. Healthy People Statistics notes, no. 20. Hyattsville: National Center for Health Statistics; 2001.
46.
47.
go back to reference Yong PL, Boyle J, Ballow M, Boyle M, Berger M, Bleesing J, et al. Use of intravenous immunoglobulin and adjunctive therapies in the treatment of primary immunodeficiencies: a working group report of and study by the Primary Immunodeficiency Committee of the American Academy of Allergy Asthma and Immunology. Clin Immunol. 2010;135(2):255–63.PubMedCrossRef Yong PL, Boyle J, Ballow M, Boyle M, Berger M, Bleesing J, et al. Use of intravenous immunoglobulin and adjunctive therapies in the treatment of primary immunodeficiencies: a working group report of and study by the Primary Immunodeficiency Committee of the American Academy of Allergy Asthma and Immunology. Clin Immunol. 2010;135(2):255–63.PubMedCrossRef
48.
go back to reference Hernandez-Trujillo HS, Chapel H, Lo Re 3rd V, Notarangelo LD, Gathmann B, Grimbacher B, et al. Comparison of American and European practices in the management of patients with primary immunodeficiencies. Clin Exp Immunol. 2012;169(1):57–69.PubMedCentralPubMedCrossRef Hernandez-Trujillo HS, Chapel H, Lo Re 3rd V, Notarangelo LD, Gathmann B, Grimbacher B, et al. Comparison of American and European practices in the management of patients with primary immunodeficiencies. Clin Exp Immunol. 2012;169(1):57–69.PubMedCentralPubMedCrossRef
49.
go back to reference Lucas M, Lee M, Lortan J, Lopez-Granados E, Misbah S, Chapel H. Infection outcomes in patients with common variable immunodeficiency disorders: relationship to immunoglobulin therapy over 22 years. J Allergy Clin Immunol. 2010;125(6):1354–60.PubMedCrossRef Lucas M, Lee M, Lortan J, Lopez-Granados E, Misbah S, Chapel H. Infection outcomes in patients with common variable immunodeficiency disorders: relationship to immunoglobulin therapy over 22 years. J Allergy Clin Immunol. 2010;125(6):1354–60.PubMedCrossRef
50.
52.
go back to reference Elovaara I, Apostolski S, van Doorn P, Gilhus NE, Hietaharju A, Honkaniemi J, et al. EFNS guidelines for the use of intravenous immunoglobulin in treatment of neurological diseases: EFNS task force on the use of intravenous immunoglobulin in treatment of neurological diseases. Eur J Neurol. 2008;15(9):893–908.PubMedCrossRef Elovaara I, Apostolski S, van Doorn P, Gilhus NE, Hietaharju A, Honkaniemi J, et al. EFNS guidelines for the use of intravenous immunoglobulin in treatment of neurological diseases: EFNS task force on the use of intravenous immunoglobulin in treatment of neurological diseases. Eur J Neurol. 2008;15(9):893–908.PubMedCrossRef
53.
go back to reference Patwa HS, Chaudhry V, Katzberg H, Rae-Grant AD, So YT. Evidence-based guideline: intravenous immunoglobulin in the treatment of neuromuscular disorders: report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology. Neurology. 2012;78(13):1009–15.PubMedCrossRef Patwa HS, Chaudhry V, Katzberg H, Rae-Grant AD, So YT. Evidence-based guideline: intravenous immunoglobulin in the treatment of neuromuscular disorders: report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology. Neurology. 2012;78(13):1009–15.PubMedCrossRef
54.
go back to reference Bonilla FA, Bernstein IL, Khan DA, Ballas ZK, Chinen J, Frank MM, et al. Practice parameter for the diagnosis and management of primary immunodeficiency. Ann Allergy Asthma Immunol. 2005;94(5 Suppl 1):S1–S63.PubMedCrossRef Bonilla FA, Bernstein IL, Khan DA, Ballas ZK, Chinen J, Frank MM, et al. Practice parameter for the diagnosis and management of primary immunodeficiency. Ann Allergy Asthma Immunol. 2005;94(5 Suppl 1):S1–S63.PubMedCrossRef
55.
go back to reference Roifman CM, Levison H, Gelfand EW. High-dose versus low-dose intravenous immunoglobulin in hypogammaglobulinaemia and chronic lung disease. Lancet. 1987;1(8541):1075–7.PubMedCrossRef Roifman CM, Levison H, Gelfand EW. High-dose versus low-dose intravenous immunoglobulin in hypogammaglobulinaemia and chronic lung disease. Lancet. 1987;1(8541):1075–7.PubMedCrossRef
56.
go back to reference Liese JG, Wintergerst U, Tympner KD, Belohradsky BH. High- vs low-dose immunoglobulin therapy in the long-term treatment of X-linked agammaglobulinemia. Am J Dis Child. 1992;146(3):335–9.PubMed Liese JG, Wintergerst U, Tympner KD, Belohradsky BH. High- vs low-dose immunoglobulin therapy in the long-term treatment of X-linked agammaglobulinemia. Am J Dis Child. 1992;146(3):335–9.PubMed
57.
go back to reference Eijkhout HW, van Der Meer JW, Kallenberg CG, Weening RS, van Dissel JT, Sanders LA, et al. The effect of two different dosages of intravenous immunoglobulin on the incidence of recurrent infections in patients with primary hypogammaglobulinemia. A randomized, double-blind, multicenter crossover trial. Ann Intern Med. 2001;135(3):165–74.PubMedCrossRef Eijkhout HW, van Der Meer JW, Kallenberg CG, Weening RS, van Dissel JT, Sanders LA, et al. The effect of two different dosages of intravenous immunoglobulin on the incidence of recurrent infections in patients with primary hypogammaglobulinemia. A randomized, double-blind, multicenter crossover trial. Ann Intern Med. 2001;135(3):165–74.PubMedCrossRef
58.
go back to reference Berger M. Incidence of infection is inversely related to steady-state (Trough) serum IgG level in studies of subcutaneous IgG in PIDD. J Clin Immunol. 2011;31(5):924–6.PubMedCrossRef Berger M. Incidence of infection is inversely related to steady-state (Trough) serum IgG level in studies of subcutaneous IgG in PIDD. J Clin Immunol. 2011;31(5):924–6.PubMedCrossRef
59.
go back to reference Quinti I, Soresina A, Guerra A, Rondelli R, Spadaro G, Agostini C, et al. Effectiveness of immunoglobulin replacement therapy on clinical outcome in patients with primary antibody deficiencies: results from a multicenter prospective cohort study. J Clin Immunol. 2011;31(3):315–22.PubMedCrossRef Quinti I, Soresina A, Guerra A, Rondelli R, Spadaro G, Agostini C, et al. Effectiveness of immunoglobulin replacement therapy on clinical outcome in patients with primary antibody deficiencies: results from a multicenter prospective cohort study. J Clin Immunol. 2011;31(3):315–22.PubMedCrossRef
60.
go back to reference Carsetti R, Rosado MM, Donnanno S, Guazzi V, Soresina A, Meini A, et al. The loss of IgM memory B cells correlates with clinical disease in common variable immunodeficiency. J Allergy Clin Immunol. 2005;115(2):412–7.PubMedCrossRef Carsetti R, Rosado MM, Donnanno S, Guazzi V, Soresina A, Meini A, et al. The loss of IgM memory B cells correlates with clinical disease in common variable immunodeficiency. J Allergy Clin Immunol. 2005;115(2):412–7.PubMedCrossRef
61.
go back to reference Chapel H, Lucas M, Lee M, Bjorkander J, Webster D, Grimbacher B, et al. Common variable immunodeficiency disorders: division into distinct clinical phenotypes. Blood. 2008;112(2):277–86.PubMedCrossRef Chapel H, Lucas M, Lee M, Bjorkander J, Webster D, Grimbacher B, et al. Common variable immunodeficiency disorders: division into distinct clinical phenotypes. Blood. 2008;112(2):277–86.PubMedCrossRef
62.
go back to reference Chapel H, Cunningham-Rundles C. Update in understanding common variable immunodeficiency disorders (CVIDs) and the management of patients with these conditions. Br J Haematol. 2009;145(6):709–27.PubMedCentralPubMedCrossRef Chapel H, Cunningham-Rundles C. Update in understanding common variable immunodeficiency disorders (CVIDs) and the management of patients with these conditions. Br J Haematol. 2009;145(6):709–27.PubMedCentralPubMedCrossRef
63.
go back to reference Chapel H, Lucas M, Patel S, Lee M, Cunningham-Rundles C, Resnick E. Confirmation and improvement of criteria for clinical phenotyping in common variable immunodeficiency disorders in replicate cohorts. J Allergy Clin Immunol. 2012;130(5):1197–1198e9.PubMedCrossRef Chapel H, Lucas M, Patel S, Lee M, Cunningham-Rundles C, Resnick E. Confirmation and improvement of criteria for clinical phenotyping in common variable immunodeficiency disorders in replicate cohorts. J Allergy Clin Immunol. 2012;130(5):1197–1198e9.PubMedCrossRef
64.
go back to reference Orange JS, Ballow M, Stiehm ER, Ballas ZK, Chinen J, De La Morena M, et al. Use and interpretation of diagnostic vaccination in primary immunodeficiency: a working group report of the Basic and Clinical Immunology Interest Section of the American Academy of Allergy, Asthma & Immunology Genome-wide association identifies diverse causes of common variable immunodeficiency. J Allergy Clin Immunol. 2012;130:S1–S24.PubMedCrossRef Orange JS, Ballow M, Stiehm ER, Ballas ZK, Chinen J, De La Morena M, et al. Use and interpretation of diagnostic vaccination in primary immunodeficiency: a working group report of the Basic and Clinical Immunology Interest Section of the American Academy of Allergy, Asthma & Immunology Genome-wide association identifies diverse causes of common variable immunodeficiency. J Allergy Clin Immunol. 2012;130:S1–S24.PubMedCrossRef
65.
go back to reference Wehr C, Kivioja T, Schmitt C, Ferry B, Witte T, Eren E, et al. The EUROclass trial: defining subgroups in common variable immunodeficiency. Blood. 2008;111(1):77–85.PubMedCrossRef Wehr C, Kivioja T, Schmitt C, Ferry B, Witte T, Eren E, et al. The EUROclass trial: defining subgroups in common variable immunodeficiency. Blood. 2008;111(1):77–85.PubMedCrossRef
66.
go back to reference Orange JS, Glessner JT, Resnick E, Sullivan KE, Lucas M, Ferry B, et al. Genome-wide association identifies diverse causes of common variable immunodeficiency. J Allergy Clin Immunol. 2011;127:1360–7.PubMedCentralPubMedCrossRef Orange JS, Glessner JT, Resnick E, Sullivan KE, Lucas M, Ferry B, et al. Genome-wide association identifies diverse causes of common variable immunodeficiency. J Allergy Clin Immunol. 2011;127:1360–7.PubMedCentralPubMedCrossRef
67.
go back to reference Stonebraker JS, Farrugia A, Gathmann B. A decision analysis model to estimate latent therapeutic demand for immunoglobulin therapy in primary immunodeficiencies. Proceedings of the 15th Meeting of the European Society of Immunodeficiencies—ESID (October 3–6, 2012, Florence, Italy). 2013;29–34. Stonebraker JS, Farrugia A, Gathmann B. A decision analysis model to estimate latent therapeutic demand for immunoglobulin therapy in primary immunodeficiencies. Proceedings of the 15th Meeting of the European Society of Immunodeficiencies—ESID (October 3–6, 2012, Florence, Italy). 2013;29–34.
68.
go back to reference Schöndorf I. Resolving barriers to the treatment of primary immunodeficiencies. The Source. 2011;19–20. Schöndorf I. Resolving barriers to the treatment of primary immunodeficiencies. The Source. 2011;19–20.
Metadata
Title
Modeling Primary Immunodeficiency Disease Epidemiology and Its Treatment to Estimate Latent Therapeutic Demand for Immunoglobulin
Authors
Jeffrey S. Stonebraker
Albert Farrugia
Benjamin Gathmann
Jordan S. Orange
ESID Registry Working Party
Publication date
01-02-2014
Publisher
Springer US
Published in
Journal of Clinical Immunology / Issue 2/2014
Print ISSN: 0271-9142
Electronic ISSN: 1573-2592
DOI
https://doi.org/10.1007/s10875-013-9975-1

Other articles of this Issue 2/2014

Journal of Clinical Immunology 2/2014 Go to the issue