TABLE 1. Summary of 149 immunodeficiency-associated vaccine-derived poliovirus (iVDPV) cases reported in the World Health Organization (WHO) iVDPV registry — worldwide, January 1, 1961–December 31, 2019*.
Characteristic | No. (%) |
---|---|
iVDPV cases reported to WHO (1961–2019) |
149 (100) |
Period detected
| |
1961–2000 |
19 (12.8) |
2001–2010 |
31 (20.8) |
2011–2020 |
99 (66.4) |
WHO region
| |
African |
10 (6.7) |
Eastern Mediterranean |
74 (49.7) |
European |
16 (10.7) |
Americas |
18 (12.1) |
South-East Asian |
15 (10.1) |
Western Pacific |
16 (10.7) |
Sex
| |
Female |
64 (40.6) |
Male |
85 (59.4) |
Acute flaccid paralysis
| |
Yes |
95 (63.8) |
No |
51 (34.2) |
Unknown |
3 (2.0) |
Age group at onset (yrs)
| |
<1 |
86 (59.3) |
1–5 |
40 (27.6) |
>5 |
19 (13.1) |
Immunodeficiency category
| |
Antibody disorders (HGG, AGG, XLA) |
39 (28.1) |
Common variable immunodeficiency |
22 (15.8) |
SCID and other combined humoral/T-cell deficiencies |
46 (33.1) |
Other (MHC class II deficiency, centromere instability, ICF syndrome) |
20 (14.4) |
Unknown |
12 (8.6) |
Serotype
| |
1 |
27 (18.1) |
2 |
83 (55.7) |
3 |
33 (22.1) |
1 and 2 |
3 (2.0) |
2 and 3 |
3 (2.0) |
Outcome
| |
Alive |
16 (10.7) |
Alive and stopped excreting |
52 (34.9) |
Dead |
65 (43.6) |
Unknown/Lost to follow-up | 16 (10.7) |
Abbreviations: AGG = agammaglobulinemia; HGG = hypogammaglobulinemia; ICF = centromeric region instability, facial anomalies syndrome; MHC = major histocompatibility complex; SCID = severe combined immunodeficiency; XLA = X-linked agammaglobulinemia.
*Data as of May 17, 2020.