TNF-α inhibitors and vaccinations: Comparison
View Latest Version
Please note this is a comparison between Version 1 by Giulio Rizzetto and Version 2 by Catherine Yang.

This entry is a up-to-dated review of the current indications for vaccination in patients on anti-TNF-a therapy. Live attenuated vaccines are always contraindicated, while inactivated vaccines can be safely administered.

This article is a up-to-dated review of the current indications for vaccination in patients on anti-TNF-a therapy. Live attenuated vaccines are always contraindicated, while inactivated vaccines can be safely administered.

  • TNF-α inhibitors

1. Introduction

TNF-α inhibitors are an important treatment option for moderate-to-severe plaque psoriasis [1]. The evaluation of safety and efficacy in developing an adequate immune response to pneumococcal polysaccharide and inactivated influenza vaccine has been conducted in patients with rheumatoid arthritis and psoriatic arthritis [2][3][4][5][6][7]. Treatment with etanercept, adalimumab and infliximab was shown not to affect the response to the pneumococcal vaccine. Concomitant use of methotrexate (MTX) or disease-modifying antirheumatic drugs (DMARDs) may result in a lower antibody response to the pneumococcal polysaccharide vaccine, although they do not alter the response to the inactivated influenza vaccine [2][8]. These two vaccinations are very important in patients receiving anti-TNF therapy to reduce complications related to those infections.

The administration of live attenuated vaccines is contraindicated in concomitance with TNF-α inhibitors due to the increased infectious risk and lack of available data. However, one study by Suissa et al. [9] showed a possible protective role of etanercept in exacerbations of chronic obstructive pulmonary disease, making it the first choice in patients at particularly high infectious risk or receiving a live attenuated vaccine.

Transplacental passage of IgG occurs in pregnant women on anti-TNF-α therapy during the third trimester and anti-TNF-α IgG has been found up to 6 months after birth in an infant [10]. For this reason, live attenuated vaccines should be avoided for the first six months in infants of mothers treated with TNF-α inhibitors [11], with the exception of certolizumab pegol [12]. In fact, one death from disseminated tuberculosis occurred in an infant exposed to infliximab and vaccinated with Bacillus Calmette–Guérin [13]. TNF-α inhibitors that can cross the blood-placental barrier can also be excreted in breast milk, so breastfeeding should be avoided if therapy cannot be discontinued [14]. The newborn vaccination schedule should be re-evaluated in the event of exposure to anti-TNF-α therapy, possibly by assessing the serum level of the biologic considered prior to administration of a live-attenuated vaccine [15].

2. Certolizumab

1. Certolizumab

Certolizumab pegol is a pegylated Fab fragment of a monoclonal antibody targeting TNF-α, indicated in moderate-to-severe plaque psoriasis

[16]

. In the literature, a randomized phase IV trial on 224 subjects confirmed the efficacy and safety of inactivated trivalent influenza and polysaccharide pneumococcal vaccination in patients with rheumatoid arthritis treated with certolizumab pegol, reporting a humoral response comparable to placebo patients. Lower antibody responses were seen in patients treated with anti-TNF-α and concomitant DMARD (MTX)

[17].

.

3. Adalimumab

2. Adalimumab

Adalimumab is a monoclonal antibody that inhibits the action of TNF-a. In the literature, a randomized, multi-center, double-blind clinical trial involving 226 adult subjects with rheumatoid arthritis reported similar antibody responses to trivalent influenza virus vaccine and 23-valent pneumococcal vaccine in subjects treated with adalimumab or placebo [3]. This underlines the efficacy and safety of vaccination with both pneumococcal capsular polysaccharide antigens and inactivated influenza vaccine.

In a study by Burmester et al. [18], 15,132 patients with rheumatoid arthritis treated with adalimumab were analyzed. Of these, 351 patients received influenza vaccination, reporting fewer infection-related adverse effects than unvaccinated subjects.

No data are available on secondary transmission of infection from live vaccines in patients receiving adalimumab but, given the increased risk of infection, administration is not recommended [19].

As for pediatric patients, it is recommended to administer adalimumab after having performed the vaccinations required for age. Administration of live and live-attenuated vaccines to children exposed to adalimumab in utero is not recommended until five months after the last administration of adalimumab to the mother during pregnancy [20][21].

43. Etanercept

Etanercept is a dimer consisting of a protein corresponding to the extracellular domain of TNF-a receptor 2 and the Fc fraction of human IgG1 immunoglobulin.

[22]

Since no studies are available concerning the infectious risk from live vaccines, their administration in patients receiving etanercept is not recommended. In a randomised,

[22]

double-blind, placebo-controlled clinical trial in patients with psoriatic arthritis, 184 patients received a multivalent polysaccharide pneumococcal vaccine at week 4 of etanercept treatment. In this study, most patients treated with etanercept were able to produce an effective B-cell immune response to the pneumococcal polysaccharide vaccine.

In a study by

Rákóczi et al

[23]

, the 4- and 8-week immunogenicity of a 13-valent pneumococcal vaccine was evaluated in rheumatoid arthritis patients treated with etanercept and methotrexate (15) or with etanercept alone (7) or with NSAIDs alone (24), confirming the efficacy of the antibody response and the safety of the vaccine in all patients treated with etanercept.

54. Infliximab

Infliximab is a IgG1 monoclonal antibody that bind TNF-a. The concomitant administration of live vaccines with infliximab is not recommended. In infants exposed in utero to infliximab, a fatal outcome due to disseminated bacillus Calmette-Guérin (BCG) infection has been reported after administration of BCG vaccine after birth. A waiting period of at least six months after birth is recommended before administering live vaccines to infants exposed in utero to infliximab.

[24]

In a study concerning pneumococcal vaccination (pneumovax) in rheumatoid arthritis patients treated with infliximab and methotrexate it was shown that infliximab did not alter the antibody response, although in all patients treated with methotrexate the antibody title was lower than in untreated subjects.

[25]

A randomised study by

deBruyn et al

.

[26]

in 134 patients with inflammatory bowel disease (IBD) treated with infliximab confirms that infliximab does not alter the antibody response of the influenza vaccine, even in relation to the timing of infusion. Recently,

Caldera et al

.

[27] showed an increased antibody response in IBD patients treated with infliximab following a high dose influenza vaccine compared to the standard dose.

showed an increased antibody response in IBD patients treated with infliximab following a high dose influenza vaccine compared to the standard dose.

 

 

 

 

References

  1. Campanati, A.; Paolinelli, M.; Diotallevi, F.; Martina, E.; Molinelli, E.; Offidani, A. Pharmacodynamics OF TNF α inhibitors for the treatment of psoriasis. Expert Opin. Drug Metab. Toxicol. 2019, 15, 913–925.
  2. Kapetanovic, M.C.; Saxne, T.; Sjoholm, A.; Truedsson, L.; Jonsson, G.; Geborek, P. Influence of methotrexate, TNF blockers and prednisolone on antibody responses to pneumococcal polysaccharide vaccine in patients with rheumatoid arthritis. Rheumatology 2006, 45, 106–111.
  3. Kaine, J.L.; Kivitz, A.J.; Birbara, C.; Luo, A.Y. Immune responses following administration of influenza and pneumococcal vaccines to patients with rheumatoid arthritis receiving adalimumab. J. Rheumatol. 2007, 34, 272–279.
  4. Brezinschek, H.P.; Hofstaetter, T.; Leeb, B.F.; Haindl, P.; Graninger, W.B. Immunization of patients with rheumatoid arthritis with antitumor necrosis factor alpha therapy and methotrexate. Curr. Opin. Rheumatol. 2008, 20, 295–299.
  5. Elkayam, O.; Paran, D.; Caspi, D.; Litinsky, I.; Yaron, M.; Charboneau, D.; Rubins, J.B. Immunogenicity and safety of pneumococcal vaccination in patients with rheumatoid ar-thritis or systemic lupus erythematosus. Clin. Infect. Dis. 2002, 34, 147–153.
  6. Broyde, A.; Arad, U.; Madar-Balakirski, N.; Paran, D.; Kaufman, I.; Levartovsky, D.; Wigler, I.; Caspi, D.; Elkayam, O. Longterm Efficacy of an Antipneumococcal Polysaccharide Vaccine among Patients with Autoimmune Inflammatory Rheumatic Diseases. J. Rheumatol. 2016, 43, 267–272.
  7. Ding, T.; Ledingham, J.; Luqmani, R.; Westlake, S.; Hyrich, K.; Lunt, M.; Kiely, P.; Bukhari, M.; Abernethy, R.; Bosworth, A.; et al. BSR and BHPR rheumatoid arthritis guidelines on safety of anti-TNF therapies. Rheumatology 2010, 49, 2217–2219.
  8. Chalmers, A.; Scheifele, D.; Patterson, C.; Williams, D.; Weber, J.; Shuckett, R.; Teufel, A. Immunization of patients with rheumatoid arthritis against influenza: A study of vaccine safety and immunogenicity. J. Rheumatol. 1994, 21, 1203–1206.
  9. Suissa, S.; Ernst, P.; Hudson, M. TNF-α antagonists and the prevention of hospitalisation for chronic obstructive pulmonary disease. Pulm. Pharmacol. Ther. 2008, 21, 234–238.
  10. Julsgaard, M.; Christensen, L.A.; Gibson, P.R.; Gearry, R.B.; Fallingborg, J.; Hvas, C.L.; Bibby, B.M.; Uldbjerg, N.; Connell, W.R.; Rosella, O.; et al. Concentrations of Adalimumab and Infliximab in Mothers and Newborns, and Effects on Infection. Gastroenterology 2016, 151, 110–119.
  11. Mahadevan, U.; Wolf, D.C.; Dubinsky, M.; Cortot, A.; Lee, S.D.; Siegel, C.A.; Ullman, T.; Glover, S.; Valentine, J.F.; Rubin, D.T.; et al. Placental Transfer of Anti–Tumor Necrosis Factor Agents in Pregnant Patients With Inflammatory Bowel Disease. Clin. Gastroenterol. Hepatol. 2013, 11, 286–292.
  12. Mariette, X.; Förger, F.; Abraham, B.; Flynn, A.D.; Moltó, A.; Flipo, R.-M.; Van Tubergen, A.; Shaughnessy, L.; Simpson, J.; Teil, M.; et al. Lack of placental transfer of certolizumab pegol during pregnancy: Results from CRIB, a prospective, postmarketing, pharmacokinetic study. Ann. Rheum. Dis. 2018, 77, 228–233.
  13. Cheent, K.; Nolan, J.; Shariq, S.; Kiho, L.; Pal, A.; Arnold, J. Case Report: Fatal case of disseminated BCG infection in an infant born to a mother taking infliximab for Crohn’s Disease. J. Crohns Coliti 2010, 4, 603–605.
  14. Gisbert, J.P.; Chaparro, M. Safety of Anti-TNF Agents during Pregnancy and Breastfeeding in Women With Inflammatory Bowel Disease. Am. J. Gastroenterol. 2013, 108, 1426–1438.
  15. Götestam, S.C.; Hoeltzenbein, M.; Tincani, A.; Fischer-Betz, R.; Elefant, E.; Chambers, C.; da Silva, J.; Nelson-Piercy, C.; Cetin, I.; Costedoat-Chalumeau, N.; et al. The EULAR points to consider for use of antirheumatic drugs before pregnancy, and during pregnancy and lactation. Ann. Rheum. Dis. 2016, 75, 795–810.
  16. Blauvelt, A.; Paul, C.; Van De Kerkhof, P.; Warren, R.; Gottlieb, A.; Langley, R.; Brock, F.; Arendt, C.; Boehnlein, M.; Lebwohl, M.; et al. Long-term safety of certolizumab pegol in plaque psoriasis: Pooled analysis over 3 years from three phase III, randomized, placebo-controlled studies. Br. J. Dermatol. 2020.
  17. Kivitz, A.J.; Schechtman, J.; Texter, M.; Fichtner, A.; De Longueville, M.; Chartash, E.K. Vaccine Responses in Patients with Rheumatoid Arthritis Treated with Certolizumab Pegol: Results from a Single-blind Randomized Phase IV Trial. J. Rheumatol. 2014, 41, 648–657.
  18. Burmester, G.R.; Landewé, R.; Genovese, M.C.; Friedman, A.W.; Pfeifer, N.D.; A Varothai, N.; Lacerda, A.P. Adalimumab long-term safety: Infections, vaccination response and pregnancy outcomes in patients with rheumatoid arthritis. Ann. Rheum. Dis. 2017, 76, 414–417.
  19. Humira Prescribing Information. Available online: (accessed on 10 December 2020).
  20. Van Assen, S.; Agmon-Levin, N.; Elkayam, O.; Cervera, R.; Doran, M.F.; Dougados, M.; Emery, P.; Geborek, P.; Ioannidis, J.P.A.; Jayne, D.R.W.; et al. EULAR recommendations for vaccination in adult patients with autoimmune inflammatory rheumatic diseases. Ann. Rheum. Dis. 2011, 70, 414–422.
  21. Di Lernia, V.; Bianchi, L.; Guerriero, C.; Stingeni, L.; Gisondi, P.; Filoni, A.; Guarneri, C.; Belloni Fortina, A.; Lasagni, C.; Simonetti, O.; et al. Adalimumab in severe plaque psoriasis of childhood: A multi-center, retrospective real-life study up to 52 weeks observation. Dermatol. Ther. 2019, 32, e13091.
  22. Mease PJ, Ritchlin CT, Martin RW, Gottlieb AB, Baumgartner SW, Burge DJ, Whitmore JB. Pneumococcal vaccine response in psoriatic arthritis patients during treatment with etanercept. J Rheumatol. 2004 Jul;31(7):1356-61. PMID: 15229957.
  23. Rákóczi É, Perge B, Végh E, Csomor P, Pusztai A, Szamosi S, Bodnár N, Szántó S, Szücs G, Szekanecz Z. Evaluation of the immunogenicity of the 13-valent conjugated pneumococcal vaccine in rheumatoid arthritis patients treated with etanercept. Joint Bone Spine. 2016 Dec;83(6):675-679. doi: 10.1016/j.jbspin.2015.10.017. Epub 2016 Mar 16. PMID: 26995488.
  24. Remicade, summary of product characteristics, accessed 14 Apr 2021 https://www.ema.europa.eu/en/documents/product-information/remicade-epar-product-information_en.pdf
  25. Visvanathan S, Keenan GF, Baker DG, Levinson AI, Wagner CL. Response to pneumococcal vaccine in patients with early rheumatoid arthritis receiving infliximab plus methotrexate or methotrexate alone. J Rheumatol. 2007 May;34(5):952-7. Epub 2007 Apr 15. PMID: 17444589.
  26. deBruyn J, Fonseca K, Ghosh S, Panaccione R, Gasia MF, Ueno A, Kaplan GG, Seow CH, Wrobel I. Immunogenicity of Influenza Vaccine for Patients with Inflammatory Bowel Disease on Maintenance Infliximab Therapy: A Randomized Trial. Inflamm Bowel Dis. 2016 Mar;22(3):638-47.
  27. Caldera F, Hillman L, Saha S, Wald A, Grimes I, Zhang Y, Sharpe AR, Reichelderfer M, Hayney MS. Immunogenicity of High Dose Influenza Vaccine for Patients with Inflammatory Bowel Disease on Anti-TNF Monotherapy: A Randomized Clinical Trial. Inflamm Bowel Dis. 2020 Mar 4;26(4):593-602. doi: 10.1093/ibd/izz164. PMID: 31504526
More
© Text is available under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/)
ScholarVision Creations
Feedback