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. 2022 Aug 30;40(41):5868–5872. doi: 10.1016/j.vaccine.2022.08.058

Table 2.

Mt. Sinai Laboratory, Ortho-Clinical VITROS, and Genscript cPASS Assay Results.

Participant
# of SARS-CoV-2 Challenges (Infection(s) and Vaccines) Prior to BT
Days Between Pre-Breakthrough Sample and Last Positive NAAT Test
Icahn SOM at Mt. Sinai Assaya
cPass Assayb
Ortho-Clinical VITROSc
1 3 NI, V2 75 51,200 98, POS 6600
2 2 UI, V2 33 800 <30, NEG 57.4
3 2 UI, V2 16 1600 58, POS 103
4f 3 NII, V1 11 1600 90, POS 116
5d 3 UI, V3 27 51,200 98, POS 6160
6d 3 UI, V3 70 51,200 98, POS 7490
7d, e 4 NI, V3 23 12,800 98, POS 2250
8d, e 4 NI, V3 36 25,600 98, POS 2710
9d 3 UI, V3 86 51,200 98, POS 13,500
10 3 NI, V2 33 6400 <30, NEG 635
11d, e 4 NI, V3 30 25,600 98, POS 4890
12d 3 UI, V3 19 6400 98, POS 1210

UI = No hx of natural infection prior to BT; NI = Hx of natural infection prior to BT; NII: Hx of natural infection 2x prior to BT; V1 = Vaccinated once; V2 = Vaccinated twice; V3 = Vaccinated twice + booster vaccination; BT = Breakthrough infection.

a

Discrete antibody titers may be reported from 1:100 to 204,800, though in this study discrete titers were only observed up to 51,200.

b

Surrogate neutralizing activity was reported from <30% to 100% (<30% = Neg, 30–100% = Pos).

c

Undiluted linear range 2–200 BAU/ml, samples diluted as needed to achieve result in linear range of 2–200 BAU/ml.

d

Received a booster vaccination.

e

Received a Moderna mRNA-1273 half dose.

f

Received Johnson & Johnson Ad26.COV2.S as primary vaccination.