| CPC G01N 33/6854 (2013.01) [G01N 21/66 (2013.01); G01N 33/54366 (2013.01); G01N 2458/30 (2013.01); G01N 2800/52 (2013.01)] | 20 Claims |

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1. A method comprising:
(i) detecting in a first biological sample obtained from a subject one or more anti-RAN protein antibodies using an electrochemiluminescence-based immunoassay;
(ii) detecting in a second biological sample obtained from the subject one or more anti-RAN protein antibodies using an electrochemiluminescence-based immunoassay, wherein the second biological sample is obtained after administration of a therapeutic agent to the subject;
(iii) comparing an amount of anti-RAN protein antibodies detected in the second biological sample to an amount of anti-RAN protein antibodies detected in the first biological sample;
(iv) identifying the subject as having a change in one or more anti-RAN protein antibody levels when the amount of anti-RAN protein antibodies detected in the second biological sample is different than the amount of anti-RAN protein antibodies detected in the first biological sample; and
(v) administering to the subject a vaccine against a RAN protein-associated disease or disorder when the second biological sample contains a decreased level of anti-RAN protein antibodies, relative to the first biological sample.
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