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. 2005 Aug 11;106(10):3343–3347. doi: 10.1182/blood-2005-02-0508

Table 2.

Epoetin rechallenge cases (n = 34 individuals) and development of epoetin responsiveness

Case no.* RIPA or ELISA antibody status at rechallenge RIPA or ELISA antibody assay Concomitant immunosuppression Neutralizing assay results at time of rechallenge Epoetin responsiveness
Group 1
    1 - RIPA + Unknown +
    2 - RIPA + - +
    3 - RIPA + - +
    4 - RIPA - - +
    5 - ELISA - Unknown -
    6 - ELISA - - +
    7 - Unknown + Unknown +
    8 - Unknown + Unknown +
    9 - Unknown - Unknown +
Group 2
    10 + RIPA + Unknown -
    11 + RIPA + Unknown -
    12 + RIPA + Unknown -
    13 + RIPA + Unknown +
    14 + RIPA + Unknown +
    15 + RIPA + - +
    16 + RIPA + - +
    17 + ELISA + Unknown -
    18 + Unknown + Unknown +
    19 + Unknown + Unknown +
    20 + Unknown + Unknown +
    21 + Unknown + Unknown -
    22 + Unknown + - +
    23 + Unknown + + -
Group 3
    24 + RIPA - Unknown -
    25 + RIPA - Unknown -
    26 + RIPA - Unknown -
    27 + RIPA - Unknown -
    28 + RIPA - Unknown -
    29 + RIPA - Unknown -
    30 + RIPA - Unknown -
    31 + RIPA - Unknown +
    32 + RIPA - Unknown +
    33 + RIPA - - +
    34 + ELISA - Unknown -

The 3 groups were defined as follows: Group 1, no evidence of antierythropoietin ELISA or RIPA antibody at the time of rechallenge; Group 2, antibodies detected and concomitant immunosuppression was administered; Group 3, antibodies detected and concomitant immunosuppression was not administered.

*

The percentage epoetin responsive were 89% for Group 1, 57% for Group 2, and 27% for Group 3.