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Erschienen in: Current Rheumatology Reports 5/2016

01.05.2016 | Infections and Arthritis (K Winthrop, Section Editor)

Fungal Infections and New Biologic Therapies

verfasst von: Snigdha Vallabhaneni, Tom M. Chiller

Erschienen in: Current Rheumatology Reports | Ausgabe 5/2016

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Abstract

The development of biologic therapies targeting proinflammatory mediators has led to significant advances in the treatment of immune-mediated inflammatory diseases (IMIDs). Blocking undesired inflammatory effects also has the potential to disrupt the body’s immune response and increase the risk for infections, including fungal infections. This review summarizes the published data on the frequency and risk for fungal infections among patients treated with biologics, with a focus on the newer therapies approved for use with IMIDs in the last 10 years. The use of biologics is associated with a small but important risk of fungal infections. Pneumocystis jirovecii pneumonia, histoplasmosis, and candidiasis are some of the most common fungal infections associated with biologics. Providers should be vigilant for fungal infection among patients taking biologics, be aware that biologic agents may alter the typical presentation of fungal infections, and take timely steps to diagnose and treat fungal infection to reduce resultant morbidity and mortality.
Literatur
1.•
Zurück zum Zitat Novosad SA, Winthrop KL. Beyond tumor necrosis factor inhibition: the expanding pipeline of biologic therapies for inflammatory diseases and their associated infectious sequelae. Clin Infect Dis. 2014;58(11):1587–98. doi:10.1093/cid/ciu104. Good overall review of many of the biologic agents and their mechanism of action, date of approval, and associated infection risk.CrossRefPubMed Novosad SA, Winthrop KL. Beyond tumor necrosis factor inhibition: the expanding pipeline of biologic therapies for inflammatory diseases and their associated infectious sequelae. Clin Infect Dis. 2014;58(11):1587–98. doi:10.​1093/​cid/​ciu104. Good overall review of many of the biologic agents and their mechanism of action, date of approval, and associated infection risk.CrossRefPubMed
2.
Zurück zum Zitat Doran MF, Crowson CS, Pond GR, et al. Frequency of infection in patients with rheumatoid arthritis compared with controls: a population-based study. Arthritis Rheum. 2002;46(9):2287–93. doi:10.1002/art.10524.CrossRefPubMed Doran MF, Crowson CS, Pond GR, et al. Frequency of infection in patients with rheumatoid arthritis compared with controls: a population-based study. Arthritis Rheum. 2002;46(9):2287–93. doi:10.​1002/​art.​10524.CrossRefPubMed
3.
Zurück zum Zitat Dixon WG, Suissa S, Hudson M. The association between systemic glucocorticoid therapy and the risk of infection in patients with rheumatoid arthritis: systematic review and meta-analyses. Arthritis Res Ther. 2011;13(4):R139. doi:10.1186/ar3453.CrossRefPubMedPubMedCentral Dixon WG, Suissa S, Hudson M. The association between systemic glucocorticoid therapy and the risk of infection in patients with rheumatoid arthritis: systematic review and meta-analyses. Arthritis Res Ther. 2011;13(4):R139. doi:10.​1186/​ar3453.CrossRefPubMedPubMedCentral
4.••
Zurück zum Zitat Kourbeti IS, Ziakas PD, Mylonakis E. Biologic therapies in rheumatoid arthritis and the risk of opportunistic infections: a meta-analysis. Clin Infect Dis. 2014;58(12):1649–57. doi:10.1093/cid/ciu185. Comprehensive analysis of risk of all opportunistic infections, including fungal infections. Particular strength is that this paper included many of the newer biologic agents.CrossRefPubMed Kourbeti IS, Ziakas PD, Mylonakis E. Biologic therapies in rheumatoid arthritis and the risk of opportunistic infections: a meta-analysis. Clin Infect Dis. 2014;58(12):1649–57. doi:10.​1093/​cid/​ciu185. Comprehensive analysis of risk of all opportunistic infections, including fungal infections. Particular strength is that this paper included many of the newer biologic agents.CrossRefPubMed
5.•
Zurück zum Zitat Baddley JW, Winthrop KL, Chen L, et al. Non-viral opportunistic infections in new users of tumour necrosis factor inhibitor therapy: results of the SAfety Assessment of Biologic ThERapy (SABER) Study. Ann Rheum Dis. 2014;73(11):1942–8. doi:10.1136/annrheumdis-2013-203407. Analysis of viral an non-viral opportunistic infections among TNF-alpha inhibitor users.CrossRefPubMedPubMedCentral Baddley JW, Winthrop KL, Chen L, et al. Non-viral opportunistic infections in new users of tumour necrosis factor inhibitor therapy: results of the SAfety Assessment of Biologic ThERapy (SABER) Study. Ann Rheum Dis. 2014;73(11):1942–8. doi:10.​1136/​annrheumdis-2013-203407. Analysis of viral an non-viral opportunistic infections among TNF-alpha inhibitor users.CrossRefPubMedPubMedCentral
7.
Zurück zum Zitat Bongartz T, Sutton AJ, Sweeting MJ, et al. Anti-TNF antibody therapy in rheumatoid arthritis and the risk of serious infections and malignancies: systematic review and meta-analysis of rare harmful effects in randomized controlled trials. JAMA. 2006;295(19):2275–85. doi:10.1001/jama.295.19.2275.CrossRefPubMed Bongartz T, Sutton AJ, Sweeting MJ, et al. Anti-TNF antibody therapy in rheumatoid arthritis and the risk of serious infections and malignancies: systematic review and meta-analysis of rare harmful effects in randomized controlled trials. JAMA. 2006;295(19):2275–85. doi:10.​1001/​jama.​295.​19.​2275.CrossRefPubMed
8.
Zurück zum Zitat Ford AC, Peyrin-Biroulet L. Opportunistic Infections With Anti-Tumor Necrosis Factor-[alpha] Therapy in Inflammatory Bowel Disease: Meta-Analysis of Randomized Controlled Trials. Am J Gastroenterol. 2013;108(8):1268–76. doi:10.1038/ajg.2013.138.CrossRefPubMed Ford AC, Peyrin-Biroulet L. Opportunistic Infections With Anti-Tumor Necrosis Factor-[alpha] Therapy in Inflammatory Bowel Disease: Meta-Analysis of Randomized Controlled Trials. Am J Gastroenterol. 2013;108(8):1268–76. doi:10.​1038/​ajg.​2013.​138.CrossRefPubMed
9.
Zurück zum Zitat Galloway JB, Hyrich KL, Mercer LK, et al. Anti-TNF therapy is associated with an increased risk of serious infections in patients with rheumatoid arthritis especially in the first 6 months of treatment: updated results from the British Society for Rheumatology Biologics Register with special emphasis on risks in the elderly. Rheumatology (Oxford). 2011;50(1):124–31. doi:10.1093/rheumatology/keq242.CrossRef Galloway JB, Hyrich KL, Mercer LK, et al. Anti-TNF therapy is associated with an increased risk of serious infections in patients with rheumatoid arthritis especially in the first 6 months of treatment: updated results from the British Society for Rheumatology Biologics Register with special emphasis on risks in the elderly. Rheumatology (Oxford). 2011;50(1):124–31. doi:10.​1093/​rheumatology/​keq242.CrossRef
10.
Zurück zum Zitat Salmon-Ceron D, Tubach F, Lortholary O, et al. Drug-specific risk of non-tuberculosis opportunistic infections in patients receiving anti-TNF therapy reported to the 3-year prospective French RATIO registry. Ann Rheum Dis. 2011;70(4):616–23. doi:10.1136/ard.2010.137422.CrossRefPubMed Salmon-Ceron D, Tubach F, Lortholary O, et al. Drug-specific risk of non-tuberculosis opportunistic infections in patients receiving anti-TNF therapy reported to the 3-year prospective French RATIO registry. Ann Rheum Dis. 2011;70(4):616–23. doi:10.​1136/​ard.​2010.​137422.CrossRefPubMed
11.
Zurück zum Zitat Tsiodras S, Samonis G, Boumpas DT, et al. Fungal infections complicating tumor necrosis factor alpha blockade therapy. Mayo Clin Proc. 2008;83(2):181–94.CrossRefPubMed Tsiodras S, Samonis G, Boumpas DT, et al. Fungal infections complicating tumor necrosis factor alpha blockade therapy. Mayo Clin Proc. 2008;83(2):181–94.CrossRefPubMed
12.
Zurück zum Zitat Lee JH, Slifman NR, Gershon SK, et al. Life-threatening histoplasmosis complicating immunotherapy with tumor necrosis factor alpha antagonists infliximab and etanercept. Arthritis Rheum. 2002;46(10):2565–70. doi:10.1002/art.10583.CrossRefPubMed Lee JH, Slifman NR, Gershon SK, et al. Life-threatening histoplasmosis complicating immunotherapy with tumor necrosis factor alpha antagonists infliximab and etanercept. Arthritis Rheum. 2002;46(10):2565–70. doi:10.​1002/​art.​10583.CrossRefPubMed
13.
Zurück zum Zitat Bergstrom L, Yocum DE, Ampel NM, et al. Increased risk of coccidioidomycosis in patients treated with tumor necrosis factor alpha antagonists. Arthritis Rheum. 2004;50(6):1959–66. doi:10.1002/art.20454.CrossRefPubMed Bergstrom L, Yocum DE, Ampel NM, et al. Increased risk of coccidioidomycosis in patients treated with tumor necrosis factor alpha antagonists. Arthritis Rheum. 2004;50(6):1959–66. doi:10.​1002/​art.​20454.CrossRefPubMed
14.
15.••
Zurück zum Zitat Salt E, Wiggins AT, Rayens MK, et al. Risk factors for targeted fungal and mycobacterial infections in patients taking TNF-alpha inhibitors. Arthritis Rheum. 2015. doi:10.1002/art.39468. This article assesses risk of fungal infection in TNF-alpha inhibitor users (not limited to IMID patients) and is one of the few studies that focuses specifically on fungal infections in this population. Salt E, Wiggins AT, Rayens MK, et al. Risk factors for targeted fungal and mycobacterial infections in patients taking TNF-alpha inhibitors. Arthritis Rheum. 2015. doi:10.​1002/​art.​39468. This article assesses risk of fungal infection in TNF-alpha inhibitor users (not limited to IMID patients) and is one of the few studies that focuses specifically on fungal infections in this population.
17.
Zurück zum Zitat Sandborn WJ, Lee SD, Randall C, et al. Long-term safety and efficacy of certolizumab pegol in the treatment of Crohn’s disease: 7-year results from the PRECiSE 3 study. Aliment Pharmacol Ther. 2014;40(8):903–16. doi:10.1111/apt.12930.CrossRefPubMed Sandborn WJ, Lee SD, Randall C, et al. Long-term safety and efficacy of certolizumab pegol in the treatment of Crohn’s disease: 7-year results from the PRECiSE 3 study. Aliment Pharmacol Ther. 2014;40(8):903–16. doi:10.​1111/​apt.​12930.CrossRefPubMed
19.
Zurück zum Zitat Donahue KE, Jonas DE, Hansen RA, et al. AHRQ comparative effectiveness reviews. Drug therapy for rheumatoid arthritis in adults: an update. . 2012. Donahue KE, Jonas DE, Hansen RA, et al. AHRQ comparative effectiveness reviews. Drug therapy for rheumatoid arthritis in adults: an update. . 2012.
20.
Zurück zum Zitat Kay J, Fleischmann R, Keystone E, et al. Golimumab 3-year safety update: an analysis of pooled data from the long-term extensions of randomised, double-blind, placebo-controlled trials conducted in patients with rheumatoid arthritis, psoriatic arthritis or ankylosing spondylitis. Ann Rheum Dis. 2015;74(3):538–46. doi:10.1136/annrheumdis-2013-204195.CrossRefPubMedPubMedCentral Kay J, Fleischmann R, Keystone E, et al. Golimumab 3-year safety update: an analysis of pooled data from the long-term extensions of randomised, double-blind, placebo-controlled trials conducted in patients with rheumatoid arthritis, psoriatic arthritis or ankylosing spondylitis. Ann Rheum Dis. 2015;74(3):538–46. doi:10.​1136/​annrheumdis-2013-204195.CrossRefPubMedPubMedCentral
26.
Zurück zum Zitat Lee YH, Bae SC. Comparative efficacy and safety of tocilizumab, rituximab, abatacept and tofacitinib in patients with active rheumatoid arthritis that inadequately responds to tumor necrosis factor inhibitors: a Bayesian network meta-analysis of randomized controlled trials. Int J Rheum Dis. 2015. doi:10.1111/1756-185x.12822. Lee YH, Bae SC. Comparative efficacy and safety of tocilizumab, rituximab, abatacept and tofacitinib in patients with active rheumatoid arthritis that inadequately responds to tumor necrosis factor inhibitors: a Bayesian network meta-analysis of randomized controlled trials. Int J Rheum Dis. 2015. doi:10.​1111/​1756-185x.​12822.
28.
Zurück zum Zitat Lovell DJ, Ruperto N, Mouy R, et al. Long-term safety, efficacy, and quality of life in patients with juvenile idiopathic arthritis treated with intravenous abatacept for up to seven years. Arthritis Rheum. 2015;67(10):2759–70. doi:10.1002/art.39234.CrossRef Lovell DJ, Ruperto N, Mouy R, et al. Long-term safety, efficacy, and quality of life in patients with juvenile idiopathic arthritis treated with intravenous abatacept for up to seven years. Arthritis Rheum. 2015;67(10):2759–70. doi:10.​1002/​art.​39234.CrossRef
29.
Zurück zum Zitat Kremer JM, Peterfy C, Russell AS, et al. Long term safety, efficacy, and inhibition of structural damage progression over 5 years of treatment with abatacept in patients with rheumatoid arthritis in the abatacept in inadequate responders to methotrexate trial. J Rheumatol. 2014;41(6):1077–87. doi:10.3899/jrheum.130263.CrossRefPubMed Kremer JM, Peterfy C, Russell AS, et al. Long term safety, efficacy, and inhibition of structural damage progression over 5 years of treatment with abatacept in patients with rheumatoid arthritis in the abatacept in inadequate responders to methotrexate trial. J Rheumatol. 2014;41(6):1077–87. doi:10.​3899/​jrheum.​130263.CrossRefPubMed
30.
Zurück zum Zitat Alten R, Kaine J, Keystone E, et al. Long-term safety of subcutaneous abatacept in rheumatoid arthritis: integrated analysis of clinical trial data representing more than four years of treatment. Arthritis Rheum. 2014;66(8):1987–97. doi:10.1002/art.38687.CrossRef Alten R, Kaine J, Keystone E, et al. Long-term safety of subcutaneous abatacept in rheumatoid arthritis: integrated analysis of clinical trial data representing more than four years of treatment. Arthritis Rheum. 2014;66(8):1987–97. doi:10.​1002/​art.​38687.CrossRef
31.
Zurück zum Zitat Weinblatt M, Combe B, Covucci A, et al. Safety of the selective costimulation modulator abatacept in rheumatoid arthritis patients receiving background biologic and nonbiologic disease-modifying antirheumatic drugs: a one-year randomized, placebo-controlled study. Arthritis Rheum. 2006;54(9):2807–16. doi:10.1002/art.22070.CrossRefPubMed Weinblatt M, Combe B, Covucci A, et al. Safety of the selective costimulation modulator abatacept in rheumatoid arthritis patients receiving background biologic and nonbiologic disease-modifying antirheumatic drugs: a one-year randomized, placebo-controlled study. Arthritis Rheum. 2006;54(9):2807–16. doi:10.​1002/​art.​22070.CrossRefPubMed
32.
Zurück zum Zitat van Vollenhoven RF, Fleischmann RM, Furst DE, et al. Long term safety of rituximab: final report of the rheumatoid arthritis global clinical trial program over 11 years. J Rheumatol. 2015;42(10):1761–6. doi:10.3899/jrheum.150051.CrossRefPubMed van Vollenhoven RF, Fleischmann RM, Furst DE, et al. Long term safety of rituximab: final report of the rheumatoid arthritis global clinical trial program over 11 years. J Rheumatol. 2015;42(10):1761–6. doi:10.​3899/​jrheum.​150051.CrossRefPubMed
33.
Zurück zum Zitat Greenwald MW, Shergy WJ, Kaine JL, et al. Evaluation of the safety of rituximab in combination with a tumor necrosis factor inhibitor and methotrexate in patients with active rheumatoid arthritis: results from a randomized controlled trial. Arthritis Rheum. 2011;63(3):622–32. doi:10.1002/art.30194.CrossRefPubMed Greenwald MW, Shergy WJ, Kaine JL, et al. Evaluation of the safety of rituximab in combination with a tumor necrosis factor inhibitor and methotrexate in patients with active rheumatoid arthritis: results from a randomized controlled trial. Arthritis Rheum. 2011;63(3):622–32. doi:10.​1002/​art.​30194.CrossRefPubMed
34.
Zurück zum Zitat Papp K, Gottlieb AB, Naldi L, et al. Safety surveillance for ustekinumab and other psoriasis treatments from the Psoriasis Longitudinal Assessment and Registry (PSOLAR). J Drugs Dermatol. 2015;14(7):706–14.PubMed Papp K, Gottlieb AB, Naldi L, et al. Safety surveillance for ustekinumab and other psoriasis treatments from the Psoriasis Longitudinal Assessment and Registry (PSOLAR). J Drugs Dermatol. 2015;14(7):706–14.PubMed
35.
Zurück zum Zitat Papp KA, Griffiths CEM, Gordon K, et al. Long-term safety of ustekinumab in patients with moderate-to-severe psoriasis: final results from 5 years of follow-up. Br J Dermatol. 2013;168(4):844–54. doi:10.1111/bjd.12214.CrossRefPubMed Papp KA, Griffiths CEM, Gordon K, et al. Long-term safety of ustekinumab in patients with moderate-to-severe psoriasis: final results from 5 years of follow-up. Br J Dermatol. 2013;168(4):844–54. doi:10.​1111/​bjd.​12214.CrossRefPubMed
36.
Zurück zum Zitat Gordon KB, Papp KA, Langley RG, et al. Long-term safety experience of ustekinumab in patients with moderate to severe psoriasis (Part II of II): results from analyses of infections and malignancy from pooled phase II and III clinical trials. J Am Acad Dermatol. 2012;66(5):742–51. doi:10.1016/j.jaad.2011.06.041.CrossRefPubMed Gordon KB, Papp KA, Langley RG, et al. Long-term safety experience of ustekinumab in patients with moderate to severe psoriasis (Part II of II): results from analyses of infections and malignancy from pooled phase II and III clinical trials. J Am Acad Dermatol. 2012;66(5):742–51. doi:10.​1016/​j.​jaad.​2011.​06.​041.CrossRefPubMed
37.
Zurück zum Zitat Ritchlin C, Rahman P, Kavanaugh A, et al. Efficacy and safety of the anti-IL-12/23 p40 monoclonal antibody, ustekinumab, in patients with active psoriatic arthritis despite conventional non-biological and biological anti-tumour necrosis factor therapy: 6-month and 1-year results of the phase 3, multicentre, double-blind, placebo-controlled, randomised PSUMMIT 2 trial. Ann Rheum Dis. 2014;73(6):990–9. doi:10.1136/annrheumdis-2013-204655.CrossRefPubMedPubMedCentral Ritchlin C, Rahman P, Kavanaugh A, et al. Efficacy and safety of the anti-IL-12/23 p40 monoclonal antibody, ustekinumab, in patients with active psoriatic arthritis despite conventional non-biological and biological anti-tumour necrosis factor therapy: 6-month and 1-year results of the phase 3, multicentre, double-blind, placebo-controlled, randomised PSUMMIT 2 trial. Ann Rheum Dis. 2014;73(6):990–9. doi:10.​1136/​annrheumdis-2013-204655.CrossRefPubMedPubMedCentral
40.
Zurück zum Zitat Poddubnyy D, Hermann KG, Callhoff J, et al. Ustekinumab for the treatment of patients with active ankylosing spondylitis: results of a 28-week, prospective, open-label, proof-of-concept study (TOPAS). Ann Rheum Dis. 2014;73(5):817–23. doi:10.1136/annrheumdis-2013-204248.CrossRefPubMed Poddubnyy D, Hermann KG, Callhoff J, et al. Ustekinumab for the treatment of patients with active ankylosing spondylitis: results of a 28-week, prospective, open-label, proof-of-concept study (TOPAS). Ann Rheum Dis. 2014;73(5):817–23. doi:10.​1136/​annrheumdis-2013-204248.CrossRefPubMed
41.
Zurück zum Zitat Campbell L, Chen C, Bhagat SS, et al. Risk of adverse events including serious infections in rheumatoid arthritis patients treated with tocilizumab: a systematic literature review and meta-analysis of randomized controlled trials. Rheumatology (Oxford). 2011;50(3):552–62. doi:10.1093/rheumatology/keq343.CrossRef Campbell L, Chen C, Bhagat SS, et al. Risk of adverse events including serious infections in rheumatoid arthritis patients treated with tocilizumab: a systematic literature review and meta-analysis of randomized controlled trials. Rheumatology (Oxford). 2011;50(3):552–62. doi:10.​1093/​rheumatology/​keq343.CrossRef
45.
52.
Zurück zum Zitat Griffiths CE, Reich K, Lebwohl M, et al. Comparison of ixekizumab with etanercept or placebo in moderate-to-severe psoriasis (UNCOVER-2 and UNCOVER-3): results from two phase 3 randomised trials. Lancet. 2015;386(9993):541–51. doi:10.1016/s0140-6736(15)60125-8.CrossRefPubMed Griffiths CE, Reich K, Lebwohl M, et al. Comparison of ixekizumab with etanercept or placebo in moderate-to-severe psoriasis (UNCOVER-2 and UNCOVER-3): results from two phase 3 randomised trials. Lancet. 2015;386(9993):541–51. doi:10.​1016/​s0140-6736(15)60125-8.CrossRefPubMed
53.
Zurück zum Zitat Genovese MC, Braun DK, Erickson JS, et al. Safety and efficacy of open-label subcutaneous ixekizumab treatment for 48 weeks in a phase ii study in biologic-naive and TNF-IR patients with rheumatoid arthritis. J Rheumatol. 2015. doi:10.3899/jrheum.140831. Genovese MC, Braun DK, Erickson JS, et al. Safety and efficacy of open-label subcutaneous ixekizumab treatment for 48 weeks in a phase ii study in biologic-naive and TNF-IR patients with rheumatoid arthritis. J Rheumatol. 2015. doi:10.​3899/​jrheum.​140831.
54.
55.
Zurück zum Zitat Tokuda H, Sakai F, Yamada H, et al. Clinical and radiological features of Pneumocystis pneumonia in patients with rheumatoid arthritis, in comparison with methotrexate pneumonitis and Pneumocystis pneumonia in acquired immunodeficiency syndrome: a multicenter study. Intern Med. 2008;47(10):915–23.CrossRefPubMed Tokuda H, Sakai F, Yamada H, et al. Clinical and radiological features of Pneumocystis pneumonia in patients with rheumatoid arthritis, in comparison with methotrexate pneumonitis and Pneumocystis pneumonia in acquired immunodeficiency syndrome: a multicenter study. Intern Med. 2008;47(10):915–23.CrossRefPubMed
60.
Zurück zum Zitat Winthrop KL, Yamashita S, Beekmann SE, et al. Mycobacterial and Other serious infections in patients receiving anti-tumor necrosis factor and other newly approved biologic therapies: case finding through the emerging infections network. Clin Infect Dis. 2008;46(11):1738–40. doi:10.1086/587989.CrossRefPubMed Winthrop KL, Yamashita S, Beekmann SE, et al. Mycobacterial and Other serious infections in patients receiving anti-tumor necrosis factor and other newly approved biologic therapies: case finding through the emerging infections network. Clin Infect Dis. 2008;46(11):1738–40. doi:10.​1086/​587989.CrossRefPubMed
61.
Zurück zum Zitat Benedict K, Derado G, Mody R. Histoplasmosis-associated hospitalizations in the United States, 2001–2012 Open Forum Infectious Diseases. 2016 (in press). Benedict K, Derado G, Mody R. Histoplasmosis-associated hospitalizations in the United States, 2001–2012 Open Forum Infectious Diseases. 2016 (in press).
63.
Zurück zum Zitat Hage CA, Bowyer S, Tarvin SE, et al. Recognition, diagnosis, and treatment of histoplasmosis complicating tumor necrosis factor blocker therapy. Clin Infect Dis. 2010;50(1):85–92. doi:10.1086/648724.CrossRefPubMed Hage CA, Bowyer S, Tarvin SE, et al. Recognition, diagnosis, and treatment of histoplasmosis complicating tumor necrosis factor blocker therapy. Clin Infect Dis. 2010;50(1):85–92. doi:10.​1086/​648724.CrossRefPubMed
65.
Zurück zum Zitat Taroumian S, Knowles SL, Lisse JR, et al. Management of coccidioidomycosis in patients receiving biologic response modifiers or disease-modifying antirheumatic drugs. Arthritis Care Res. 2012;64(12):1903–9. doi:10.1002/acr.21784.CrossRef Taroumian S, Knowles SL, Lisse JR, et al. Management of coccidioidomycosis in patients receiving biologic response modifiers or disease-modifying antirheumatic drugs. Arthritis Care Res. 2012;64(12):1903–9. doi:10.​1002/​acr.​21784.CrossRef
Metadaten
Titel
Fungal Infections and New Biologic Therapies
verfasst von
Snigdha Vallabhaneni
Tom M. Chiller
Publikationsdatum
01.05.2016
Verlag
Springer US
Erschienen in
Current Rheumatology Reports / Ausgabe 5/2016
Print ISSN: 1523-3774
Elektronische ISSN: 1534-6307
DOI
https://doi.org/10.1007/s11926-016-0572-1

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