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Patients With Primary Immunodeficiencies Are a Reservoir of Poliovirus and a Risk to Polio Eradication Publisher



Aghamohammadi A1 ; Abolhassani H1 ; Kutukculer N2 ; Wassilak SG3 ; Pallansch MA4 ; Kluglein S5 ; Quinn J6 ; Sutter RW7 ; Wang X8, 39 ; Sanal O9 ; Latysheva T10 ; Ikinciogullari A11, 35 ; Bernatowska E12 ; Tuzankina IA13 Show All Authors
Authors
  1. Aghamohammadi A1
  2. Abolhassani H1
  3. Kutukculer N2
  4. Wassilak SG3
  5. Pallansch MA4
  6. Kluglein S5
  7. Quinn J6
  8. Sutter RW7
  9. Wang X8, 39
  10. Sanal O9
  11. Latysheva T10
  12. Ikinciogullari A11, 35
  13. Bernatowska E12
  14. Tuzankina IA13
  15. Costacarvalho BT14
  16. Franco JL15
  17. Somech R16
  18. Karakocaydiner E17
  19. Singh S18
  20. Bezrodnik L19
  21. Espinosarosales FJ20
  22. Shcherbina A21, 33
  23. Lau YL22, 23
  24. Nonoyama S24
  25. Modell F6
  26. Modell V6
  27. Ozen A17
  28. Berlin A26
  29. Chouikha A27
  30. Partidagaytan A28
  31. Kiykim A17
  32. Prakash C29
  33. Suri D30
  34. Ayvaz DC9
  35. Pelaez D31
  36. Da Silva EE32
  37. Deordieva E21, 33
  38. Perezsanchez EE34
  39. Ulusoy E2
  40. Dogu F11, 35
  41. Seminario G36
  42. Cuzcanci H9
  43. Triki H27
  44. Shimizu H37
  45. Tezcan I9
  46. Benmustapha I25, 38
  47. Sun J8, 39
  48. Mazzucchelli JTL14
  49. Orrego JC40
  50. Pac M12
  51. Bolkov M13
  52. Giraldo M40
  53. Belhajhmida N25, 38
  54. Mekki N25, 38
  55. Kuzmenko N21, 33
  56. Karaca NE2
  57. Rezaei N1
  58. Diop OM41
  59. Baris S17
  60. Chan SM42
  61. Shahmahmoodi S43
  62. Haskologlu S11, 35
  63. Ying W8, 39
  64. Wang Y8, 39
  65. Barbouche MR25, 38
  66. Mckinlay MA5

Source: Frontiers in Immunology Published:2017


Abstract

Immunodeficiency-associated vaccine-derived polioviruses (iVDPVs) have been isolated from primary immunodeficiency (PID) patients exposed to oral poliovirus vaccine (OPV). Patients may excrete poliovirus strains for months or years; the excreted viruses are frequently highly divergent from the parental OPV and have been shown to be as neurovirulent as wild virus. Thus, these patients represent a potential reservoir for transmission of neurovirulent polioviruses in the post-eradication era. In support of WHO recommendations to better estimate the prevalence of poliovirus excreters among PIDs and characterize genetic evolution of these strains, 635 patients including 570 with primary antibody deficiencies and 65 combined immunodeficiencies were studied from 13 OPV-using countries. Two stool samples were collected over 4 days, tested for enterovirus, and the poliovirus positive samples were sequenced. Thirteen patients (2%) excreted polioviruses, most for less than 2 months following identification of infection. Five (0.8%) were classified as iVDPVs (only in combined immunodeficiencies and mostly poliovirus serotype 2). Non-polio enteroviruses were detected in 30 patients (4.7%). Patients with combined immunodeficiencies had increased risk of delayed poliovirus clearance compared to primary antibody deficiencies. Usually, iVDPV was detected in subjects with combined immunodeficiencies in a short period of time after OPV exposure, most for less than 6 months. Surveillance for poliovirus excretion among PID patients should be reinforced until polio eradication is certified and the use of OPV is stopped. Survival rates among PID patients are improving in lower and middle income countries, and iVDPV excreters are identified more frequently. Antivirals or enhanced immunotherapies presently in development represent the only potential means to manage the treatment of prolonged excreters and the risk they present to the polio endgame. © 2017 Aghamohammadi, Abolhassani, Kutukculer, Wassilak, Pallansch, Kluglein, Quinn, Sutter, Wang, Sanal, Latysheva, Ikinciogullari, Bernatowska, Tuzankina, Costa-Carvalho, Franco,Somech, Karakoc-Aydiner, Singh, Bezrodnik, Espinosa-Rosales, Shcherbina, Lau, Nonoyama, Modell, Modell, Barbouche and McKinlay.
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