Across mating systems, females differ in the amount of resources they invest in offspring. For example, polyandrous females invest in acquiring multiple matings rather than providing parental care. We examined how the amount of maternal immune investment, measured as immunoglobulin Y and lysozyme activity in eggs, was influenced by female role across three social mating systems (polyandry, polygyny, and monogamy) in shorebirds. We predicted that polyandry should impose the greatest costs on the ability to provision eggs and monogamy, where females receive benefits from biparentality, the least. Contrary to our predictions, levels of maternally derived egg immune constituents were consistently high across measures in the polyandrous species and low in the monogamous species. Our results may support a link with pace-of-life where developmental costs are greater than the energetic costs of provisioning eggs, and (or) a role for sexual selection acting on maternal immune investment.