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. Author manuscript; available in PMC: 2009 Aug 5.
Published in final edited form as: Vaccine. 2008 Jun 10;26(33):4210–4217. doi: 10.1016/j.vaccine.2008.05.054

Table 1.

Demographics of subjects receiving either LAIV or TIV

Parameters Group 1 Group 2 Group 3 Groups Combined
LAIV TIV LAIV TIV LAIV TIV LAIV TIV
  Number 45 44 50 48 27 29 122 121
Gender
     Male 23 (51%) 26 (59%) 25 (50%) 28 (58%) 17 (63%) 10 (34%) 65 (53%) 64 (53%)
   Female 22 (49%) 18 (41%) 25 (50%) 20 (42%) 10 (37%) 19 (66%) 57 (47%) 57 (47%)
Ethnicity
  White1 5 (11%) 4 (9%) 7 (14%) 4 (8%) 7 (26%) 3 (10%) 20 (16%) 11 (9%)
  Black1 32 (71%) 33 (75%) 29 (58%) 32 (67%) 11 (41%) 17 (59%) 72 (59%) 82 (68%)
  Hispanic 8 (18%) 6 (14%) 13 (26%) 12 (25%) 7 (26%) 8 (28%) 27 (22%) 26 (21%)
  Others 0 (0%) 1 (2%) 1 (2%) 0 2 (7%) 1 (3%) 3 (2%) 2 (2%)
Age - years mean (STD) 13.0 (2.7) 12.2 (3.0) 10.8 (3.2) 12.2 (3.0) 9.6 (3.1) 10.9 (2.9) 11.4 (3.3) 11.9 (3.0)
Entry CD4% mean (STD) 30.7 (8.9) 31.9 (7.5) 32.9 (8.1) 32.6 (7.8) 38.0 (5.9) 39.9 (6.7) 33.2 (8.4) 34.1 (8.1)
Entry CD4 count mean (STD) 732 (328) 825 (373) 842 (344) 846 (362) 1023 (346) 1089 (349) 842 (353) 897 (376)
Entry Viral Load (Log10)* (STD) 2.8 (0.6) 2.7 (0.8) 2.7 (0.7) 2.7 (0.7) 2.6 (0.7) 2.7 (0.6) 2.7 (0.7) 2.7 (0.7)
1

non-Hispanic

*

Roche Amplicor Monitor HIV RT PCR was used for 179 subjects (if copies/ml<400, then copies/ml was set to 400); Roche UltraSensitive HIV RT PCR was used for 62 subjects (if copies/ml <50, then copies/ml was set to <500); OTC NASBA HIV RNA QT assay was used for 2 subjects (if copies/ml <500, then copies/ml was set to 500).