and then 18 million for the fifth and sixth injections. The humoral immune responses of the patients were assessed by enzyme-linked immunoadsorbent assay, radioimmunoassay, and radioimmunoprecipitation. ## RESULTS. Thirteen of the 20 patients completed the immunization protocol. Eight of these 13
Humoral immune response against melanoma antigens induced by vaccination with cytokine gene-modified autologous tumor cells
✍ Scribed by Hanno Ehlken; Dirk Schadendorf; Stefan Eichmüller
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- French
- Weight
- 133 KB
- Volume
- 108
- Category
- Article
- ISSN
- 0020-7136
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Although the existence of a humoral response against tumor‐associated antigens is well appreciated, a systematic analysis of its possible induction by the tumor remains missing. We compared the specific IgG response of Stage IV melanoma patients during vaccination. Patients had been treated within 2 clinical trials with autologous tumor cells gene‐modified for IL‐7 or IL‐12. A panel of 27 tumor‐associated antigens (HD‐MM‐01 to HD‐MM‐27) was isolated by a SEREX screening of a testis cDNA library using a pool of 5 sera from patients after vaccination. All antigens were retested with individual sera of 12 patients both pre‐ and post‐vaccination. A serological response was induced during vaccination against 18 antigens. Remarkably, induction was detected only in patients included in the screening pool. The low overlap between sero‐reactivity of the 12 patients suggested a very individualized immunological reaction. Two of 5 sera included in the screening pool exhibited a high frequency of induced humoral responses. The same patients had been shown to have a high Karnovsky index and had generated lytic cytotoxic T cells against the tumor. Besides 2 known cancer‐germline genes (SCP‐1 and PLU‐1), the other isolated antigens were expressed in a non‐tumor‐specific fashion as analyzed by virtual Northern blot or RT‐PCR. The properties of homologues to several of the identified tumor‐antigens, especially PLU‐1, SCP‐1, DNEL2, CLOCK, and PIASx‐α, suggest further investigation of their possible function in malignant melanoma. We conclude that a strong humoral response against tumor‐associated antigens is inducible by tumor cells and that this response is very individual. © 2003 Wiley‐Liss, Inc.
📜 SIMILAR VOLUMES