PROGNOSTIC SIGNIFICANCE OF THE SERUM PROTEIN CONTENT IN PREMATURE BABIES AND ITS RELATION TO PULMONARY HYALINE MEMBRANE: PRELIMINARY COMMUNICATION

1960 ◽  
Vol 1 (23) ◽  
pp. 887-888 ◽  
Author(s):  
W. D. Domville Cooke
Lung Cancer ◽  
1994 ◽  
Vol 11 ◽  
pp. 25
Author(s):  
Gianfranco Buccheri ◽  
Domenico Ferrigno

Blood ◽  
2006 ◽  
Vol 108 (11) ◽  
pp. 5044-5044
Author(s):  
Regina Stein ◽  
Jayesh Mehta ◽  
Eric Vickrey ◽  
William Resseguie ◽  
Seema Singhal

Abstract During or after therapy, patients with myeloma sometimes develop multiple protein bands that are detectable on urine/serum protein immunofixation. These so-called “oligoclonal bands” may or may not include the original monoclonal protein isotype. The phenomenon is thought to represent immune recovery with no adverse prognostic significance. Estimation of serum free light chains (SFLC) is useful in selected patients with non-secretory myeloma, and in light chain disease with anuric renal failure. The normal serum free κ:λ ratio (SFKLR) is 0.26–1.65. There are no data on SFLC levels and SFKLR in patients with oligoclonal bands. We analyzed 52 samples in 23 patients (1–6 samples per patient; median 1) with >1 monoclonal heavy and/or light chain bands on combined serum and urine immunofixation, and corresponding SFLC results. 6 samples were from 2 patients (1 and 5 samples each) known to have biclonal disease where each clone had a different light chain specificity. The remaining samples were from patients known to have a single monoclonal protein. Immunofixation on 10 (19%) samples did not show the original monoclonal protein isotype, and 42 (81%) did. 17 (33%) samples came from patients in complete remission (CR) or near-CR based on stringent conventional criteria. Based on a review of clinical and treatment history, 23 (42%) samples were classified as being from patients who had “active disease” (stable or progressive) and 29 were classified as being from patients with “inactive disease” (CR/near-CR or showing ongoing response to current therapy). SFKLR was normal in 20 (39%) samples. The table shows the relationship between SFKLR and the presence of the original paraprotein isotype, CR/near-CR, or disease activity. Subgroup Abnormal SFKLR Normal SFKLR P Original monoclonal protein 0.068 - Present 19/42 (45%) 23/42 (55%) - Absent 1/10 (10%) 9/10 (90%) Disease status 0.038 - CR/near-CR 3/17 (18%) 14/17 (82%) - Not in CR/near-CR 17/35 (49%) 18/35 (51%) Disease activity 0.10 - Inactive 14/29 (48%) 15/29 (52%) - Active 6/23 (26%) 17/23 (74%) Absence of the original monoclonal protein and CR/near-CR were significantly more likely to be associated with normal SFKLR. On the other hand, there was no significant relationship between SFKLR and disease activity. The level of monoclonal protein on serum protein electrophoresis did not correlate with SFKLR: 9 of 22 samples with monoclonal protein ≥0.2 g/dL had abnormal SFKLR compared with 11 of 30 samples with monoclonal protein <0.2 g/dL (P=0.76). Of the 6 samples from patients with known biclonal disease, 3 had normal SFKLR (1 from 1 patient and 2 from the second patient) and 3 had abnormal SFKLR (all 3 from the second patient). On the single occasion when the disease was felt to be inactive, the SFKLR was abnormal, whereas it was normal on 3 of the 5 occasions when the disease was felt to be active. This suggests that SFLC is of limited value in the uncommon situation where biclonal disease is present with both κ and λ light chains. We conclude that in myeloma patients showing multiple monoclonal bands on immunofixation on or after therapy, the presence of a normal SFKLR suggests a significantly greater likelihood of CR/near-CR.


1974 ◽  
Vol 31 (2) ◽  
pp. 219-225
Author(s):  
V. S. Jathar ◽  
R. S. Satoskar ◽  
B. M. Mehta ◽  
D. V. Rege

1. The effects of the protein content of the diet on the vitamin B12 concentration of serum and of various tissues were studied in rats by means of microbiological and radioisotopic techniques.2. Protein starvation reduced tissue weights and nitrogen contents, serum protein concentrations and haemoglobin values.3. The vitamin B12 contents of the serum and of several organs and tissues were greater in the protein-starved animals for reasons that remain unexplained.4. The retention of radioactive cyanocobalamin per g fresh weight was significantly greater in liver, kidney, spleen and brain in the protein-depleted rats than in those given adequate protein. However, the total tissue retention was not significantly different between these groups, so that there was a greater capacity for tissue binding and for body conservation of vitamin B12 in the protein-starved animals.


1962 ◽  
Vol 202 (6) ◽  
pp. 1121-1124 ◽  
Author(s):  
Lawrence I. Gottlieb ◽  
Robert D. Coye

No effect of HgCl2 poisoning on the catabolism of serum protein was noted in rabbits in which I131 was used as the protein label. The amount of I131 remaining in the perfused kidney was much greater in the poisoned animals than in the controls. This increase in label was shown to be due to an increase in the protein. Using T-1824, smaller increases were noted in the poisoned kidneys. The data are interpreted to show that the kidney is not a major site of serum protein catabolism and that the increased protein in the kidney results from increased filtration through a damaged glomerular membrane.


1951 ◽  
Vol 29 (1) ◽  
pp. 13-24
Author(s):  
Christine E. Rice ◽  
Paul Boulanger ◽  
P. J. G. Plummer

The complement and coagulative activities of the blood were studied in three groups of 20 guinea pigs each, receiving diets containing different amounts of protein, 2.3 to 26.7%. The mean complement titers were found to be lower and the prothrombin times longer in the group fed the diet containing the least protein, 2.3%. Of the four major complement components,,the fourth, C'4, appeared to be most affected. Sera of the animals receiving less protein were lower in total protein content and had lower albumin - globulin ratios than sera from guinea pigs on the higher protein diets. No relationship was demonstrated between coagulation time and serum protein content.


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