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M C Hardegree

Publications and source records attributed to M C Hardegree.

40 records · Page 3Linked to original sources

Immunization against neonatal tetanus in New Guinea. 5. Laboratory assayed potency of tetanus toxoids and relationship to human antitoxin response.

Previous papers in this series have shown that plain toxoids induced early primary antitoxin levels in women in New Guinea that were not significantly different from those induced by adsorbed toxoids but that at the end of 1 year the antitoxin levels differed significantly. Protective levels (not less than 0.01 unit/ml) induced by adsorbed toxoids persisted for more than 3 years. Results of laboratory assays of the toxoids reported in this paper show that per total human immunizing dose, the plain toxoids had 72 or less international units (IU) whereas the adsorbed toxoids had approximately 200 IU. The international "unitage" of these toxoids reflected the persistence of the human protective antitoxin level but not the early primary response. The assay results were in agreement with findings of other workers that the mouse as well as the guinea-pig may be satisfactory for potency assay of adsorbed toxoids. The need for determination of the international unitage of tetanus toxoids used in human studies and the confirmation of relationship of this value to persistence of antitoxin levels is emphasized.

Animals↗

Immunization against neonatal tetanus in New Guinea. Antitoxin response of pregnant women to adjuvant and plain toxoids.

Immunization of pregnant women in New Guinea with three injections of plain toxoid had previously been shown to prevent neonatal tetanus. In the present study antitoxin levels induced by two oil-adjuvant toxoids (one injection), one AlPO(4) toxoid (two injections) and one plain toxoid (three injections) were compared with those induced by the same plain toxoid as used in the earlier study. At term there was no significant difference in the levels for the five toxoids, but those for the plain toxoids later declined rapidly. AlPO(4)-toxoid titres were significantly higher than the titres for the plain toxoids at the end of a year, but lower than the oil-adjuvant titres, which were the highest and most persistent. However, unacceptable side-effects (induced by subsequent lots of oil-adjuvant toxoids) preclude their routine use at present.The results indicate that a maternal antitoxin level at delivery of 0.01 unit/ml is protective. Aluminium-compound toxoid rapidly achieved titres that were better than this for at least a year, with minimal side-effects. Hence such toxoids are recommended for maternal immunization to prevent neonatal tetanus.

Female↗