Hermann Lehmann

CBE FRS
Born8 July 1910 (1910-07-08)
Halle, German Empire
Died13 July 1985 (1985-07-14) (aged 75)
Cambridge, Cambridgeshire, England
CitizenshipNaturalised British
Alma materHeidelberg University
Cambridge University
Occupation(s)Biochemist, physician
Known forHemoglobin variants
Molecular anthropology
Spouse
Benigna Norman-Butler
​
​
(m. 1940)​
Children2 sons and 2 daughters
AwardsRivers Memorial Medal (1961)

Hermann Lehmann CBE FRS (8 July 1910 – 13 July 1985) was a German-born British physician and biochemist known for his works on the chemistry and diversity of hemoglobin.[1] Describing about 75 different hemoglobin, he discovered the most number of hemoglobin types than anyone else.[2] He is regarded as one of the founders of molecular anthropology.[3]

Biography

Hermann Lehmann was born in Halle, eastern Germany.[3] His father Paul Lehmann was publisher of two local newspaper. His mother Bella (née Apelt) died when he was three years old. He had three sisters and one half-brother.[1] He attended the state school at Halle for his elementary education. An economic depression, hyperinflation in the Weimar Republic, forced his father to abandon publication at Halle, and his family moved to Dresden in 1923.[1]

He completed secondary education at the Gymnasium zum heiligen Kreuz (now the Kreuzschule) in 1928. Soon after enrolling in a medical course at the University of Freiberg in Breisgau, his father died and moved to Frankfurt to live with his uncle and study there. In 1931, he entered Heidelberg University but before he complete the M.D. course, the rising anti-Semitism of Nazism compelled him to give up his final examination in 1933. Moving to Switzerland, he submitted his already finished thesis on gastric secretion titled Salzsauräproduktion in Sauglingsmagen nach Histaminreiz. Beobachtet mittels fraktionerter Ausheberung to the University of Basel. The university awarded him an M.D. in January 1934, but without medical license since his medical course was in Germany.[1]

He was appointed as a research assistant to Otto Fritz Meyerhof (winner of the Nobel Prize in Physiology and Medicine in 1922) at the Kaiser Wilhelm Institute in Heidelberg. Meyerhof arranged for his visit to the University of Cambridge in 1935, where he met Frederick Gowland Hopkins, winner of the Nobel Prize in Physiology or Medicine in 1929.[4] Hopkins invited him to move to Cambridge, and it was anecdotally said: "Gowland Hopkins told him to leave his white coat hanging behind the door of the laboratory where it would be ready for him on his return!" The same year he attended a conference at Moscow, upon the return of which he was accused of attending the Trades Union Conference.[1] As life got more difficult, he went back to England and get enrolled for a Ph.D. course in biochemistry at Christ's College, Cambridge in 1936.[3] Joseph Needham and Dorothy Needham, a researcher couple at Hopkins' laboratory helped him get a grant for Jewish refugees and let him their house.[1] Supervised by Joseph Needham, his thesis was on Aspects of carbohydrate metabolism in the absence of molecular oxygen.[5] He received the degree two years later and immediately worked under the Beit Memorial Fellowships for Medical Research until 1942.[4]

As World War II advanced, classified as a "friendly alien", he was among the Jewish refugees rounded up at Huyton in 1940. In October, he was released and volunteered himself in the work efforts. Charles Scott Sherrington, Nobel laurate and former President of the Royal Society, help him get a position in the Emergency Medical Service at Runwell Hospital in Essex. In 1942, he was recruited, again with help of Sherrington, in the Royal Army Medical Corps (R.A.M.C.) to investigate a rampant anaemia in the British Army in India. He was initially a pathologist, raised to Lieutenant Colonel and later appointed assistant director of pathology to the North East India Command. It was while working there that he received an application for naturalisation from a "certain Captain Lehmann, R.A.M.C.", to which he sent a full recommendation.[1] His major woks in the biochemistry of blood originated there as he witnessed high incidence of iron deficiency among the Indian troops. As the war ended he was demobilised in the late 1946, and was appointed in 1947 as a Senior Nutrition Research Officer under Colonial Medical Research Fellowship at Makerere College (now Makerere University) in Kampala, Uganda.[4]

In 1949, he returned to England as Consultant Pathologist at the Pembury Hospital in Kent. He moved to St Bartholomew's Hospital in London as a Senior Lecturer in 1951 and worked there until 1963. He was appointed as a biochemist at the Addenbrooke’s Hospital of the University of Cambridge in 1963. The Medical Research Council established the Abnormal Haemoglobin Research Unit under his supervision that year under the university. He eventually became the first professor of clinical biochemistry in the university in 1967.[3] Between 1963 and 1975 he was Honorary Director of the World Health Organization for the Abnormal Haemoglobin Research Unit. He retired from the university in 1977, and continued a research programme called the National Haemoglobin Reference Centre funded by WHO.[4]

In 1940, Lehmann married Benigna Norman-Butler, a musician, with whom he had two daughters, Susan and Ruth, and two sons, Paul and David.[1][4]

Scientific contributions

Lehmann was a pioneer in the study of the chemistry of blood. One of his first major contributions was on the etiology of anaemia in Uganda. At the Makerere College, he found that anaemia in many Africans was due to parasitic worm infection, specifically hookworm infection.[6][7][8] His next major work was the case of pseudocholinesterase deficiency, a deadly blood disease in which individuals have severe sensitivity to certain anesthetic drugs.[9][10] While working at St Bartholomew's Hospital, he discovered that pseudocholinesterase deficiency is the cause of idiosyncratic hypersensitivity to suxamethonium.[11] He developed biochemical test for the diagnosis,[12] and also discovered the genetic basis of the disease.[13][14][15]

Lehmanns most important works were on the variants of haemoglobins. He discovered about 75 different types of haemoglobins during his career.[2] His discoveries of haemoglobins related to blood diseases such as sickle cell disease are lasting important in medicine and biochemistry.[16] He was credited as "more than anybody responsible for cataloguing the enormous wealth of variations in the hemoglobin mutants and setting our base of understanding of the population genetics, anthropology, and clinical diversity of the structural variants."[17]

Honours and awards

Lehmann received the Darwin's Prize for his Ph.D. thesis at Christ's College in 1938.[4] He won the Rivers Memorial Medal of the Royal Anthropological Institute in 1961 for his studies of sickle cell disease in the Andaman Islands.[18] He is regarded as one of the founders of molecular anthropology.[3] He was elected a Fellow of the Christ's College in 1965, and became an honorary fellow in 1982. At Christ's College, he served as Fellows’ Steward, editor of the college magazine, and president of the College Medical Society. The University of Cambridge conferred him the degree of D.Sc. in 1957. He was an honorary professor in the University of Freiburg in 1964.[3]

He received the Martin Luther King Prize for Research on Sickle-Cell Anaemia in 1971, Conway Evans Prize of the Royal Society and Royal College of Physicians in 1976, and Wellcome Prize of the British Association for the Advancement of Science in 1978. He was elected FRS in 1972. He was elected President of the British Association for the Advancement of Science in 1972, and President of the Cambridge Philosophical Society in 1985. He was appointed Commander of the British Empire in 1980, and the National Order of the Ivory Coast in 1981.[4]

References

  1. 1 2 3 4 5 6 7 8 Dacie, John Vivian (1988). "Hermann Lehmann, 8 July 1910 - 13 July 1985". Biographical Memoirs of Fellows of the Royal Society. 34: 405–449. doi:10.1098/rsbm.1988.0015. PMID 11616113.
  2. 1 2 Huisman, T. H. J.; Efremov, G. D.; Wrightstone, R. N. (1985). "In Memoriam Professor Hermann Lehmann, CBE, FRS". Hemoglobin. 9 (5): iii–iv. doi:10.3109/03630268508997022.
  3. 1 2 3 4 5 6 Lachmann, P.J. "Hermann Lehmann". history.rcplondon.ac.uk. Retrieved 27 September 2020.
  4. 1 2 3 4 5 6 7 Rürup, Reinhard (2008). Schicksale und Karrieren Gedenkbuch für die von den Nationalsozialisten aus der Kaiser-Wilhelm-Gesellschaft vertriebenen Forscherinnen und Forscher. Göttingen: Wallstein Verlag. pp. 253–256. ISBN 978-3-89244-797-9. OCLC 237223626.
  5. ↑ "GenetiTree - Hermann Lehmann". academictree.org. Retrieved 4 October 2020.
  6. ↑ Lehmann, H. (1949). "Haemogram, serum protein and plasma volume of healthy, well-nourished East Africans in Uganda". Nature. 164 (4179): 954–955. Bibcode:1949Natur.164..954L. doi:10.1038/164954b0. PMID 15396001. S2CID 4063830.
  7. ↑ Lehmann, H. (1949). "Macrocytic anaemia in Central Africans in relation to ancylostomiasis and other diseases". Lancet. 1 (6542): 90–95. doi:10.1016/s0140-6736(49)90294-9. PMID 18106466.
  8. ↑ Lehmann, H. (1950). "The nature of macrocytic anaemia in Central Africans". Transactions of the Royal Society of Tropical Medicine and Hygiene. 43 (4): 362. PMID 15410060.
  9. ↑ Lehmann, H.; Silk, Elsie (1961). "Familial Pseudocholinesterase Deficiency". British Medical Journal. 1 (5219): 128–129. doi:10.1136/bmj.1.5219.128-b. PMC 1952834.
  10. ↑ Griffiths, P. D.; Davies, D.; Lehmann, H. (1966). "A second family demonstrating the homozygote for fluoride-resistant pseudocholinesterase variant". British Medical Journal. 2 (5507): 215–216. doi:10.1136/bmj.2.5507.215. PMC 1943181. PMID 5939099.
  11. ↑ Harris, H.; Whittaker, M.; Lehmann, H.; Silk, E. (1960). "The pseudocholinesterase variants. Esterase levels and dibucaine numbers in families selected through suxamethonium sensitive individuals". Acta Genetica et Statistica Medica. 10 (1–3): 1–16. doi:10.1159/000151112. PMID 14399955.
  12. ↑ Lehmann, H.; Davies, Daphne (1962). "Identification of the Pseudocholinesterase Type in Human Blood Spots". Medicine, Science and the Law. 2 (3): 180–183. doi:10.1177/002580246200200303. S2CID 57371918.
  13. ↑ Liddell, J.; Lehmann, H.; Silk, E. (1962). "A 'silent' pseudo-cholinesterase gene". Nature. 193 (4815): 561–562. Bibcode:1962Natur.193..561L. doi:10.1038/193561a0. PMID 14465122. S2CID 4249786.
  14. ↑ Lehmann, H.; Liddell, J. (1964). "Genetical variants of human serum pseudocholinesterase". Progress in Medical Genetics. 23: 75–105. PMID 14110078.
  15. ↑ Gaffney, P.J.; Lehmann, H. (1969). "Residual Enzyme Activity in the Serum of a Homozygote for the Silent Pseudocholinesterase Gene". Human Heredity. 19 (3): 234–238. doi:10.1159/000152224. PMID 5361486.
  16. ↑ McCurdy, P. R.; Lorkin, P. A.; Casey, R.; Lehmann, H.; Uddin, D. E.; Dickson, L. G. (1974). "Hemoglobin S-G (S-D) syndrome". The American Journal of Medicine. 57 (4): 665–670. doi:10.1016/0002-9343(74)90021-7. PMID 4432868.
  17. ↑ de Chadarevian, Soraya; Kamminga, Harmke (1998). Molecularizing Biology and Medicine: New Practices and Alliances, 1920s to 1970s. 9789057022937. Amsterdam: Harwood Academic Publishers. p. 165. ISBN 90-5702-293-1. OCLC 39155107.
  18. ↑ "Rivers Memorial Medal Prior Recipients". Royal Anthropological Institute. Retrieved 3 October 2020.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.